Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Meza-Zepeda, LA; Berner, JM; Henriksen, J; South, AP; Pedeutour, F; Dahlberg, AB; Godager, LH; Nizetic, D; Forus, A; Myklebost, O
   Ectopic sequences from truncated HMGIC in liposarcomas are derived from various amplified chromosomal regions
   GENES CHROMOSOMES & CANCER
   
   L.A. Meza-Zepeda et al., "Ectopic sequences from truncated HMGIC in liposarcomas are derived from various amplified chromosomal regions", GENE CHROM, 31(3), 2001, pp. 264-273
2. Weissenberger, AA; Dell, ML; Liow, K; Theodore, W; Frattali, CM; Hernandez, D; Zametkin, AJ
   Aggression and psychiatric comorbidity in children with hypothalamic hamartomas and their unaffected siblings
   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
   
   A.A. Weissenberger et al., "Aggression and psychiatric comorbidity in children with hypothalamic hamartomas and their unaffected siblings", J AM A CHIL, 40(6), 2001, pp. 696-703
3. Rubin, BP; Dal Cin, P
   The genetics of lipomatous tumors
   SEMINARS IN DIAGNOSTIC PATHOLOGY
   
   B.P. Rubin e P. Dal Cin, "The genetics of lipomatous tumors", SEM DIAGN P, 18(4), 2001, pp. 286-293
4. Vilgrain, V
   Cystic lesions of the liver
   GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
   
   V. Vilgrain, "Cystic lesions of the liver", GASTRO CL B, 25(4), 2001, pp. B167-B177
5. Ojeda, SR; Heger, S
   New thoughts on female precocious puberty
   JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
   
   S.R. Ojeda e S. Heger, "New thoughts on female precocious puberty", J PED END M, 14(3), 2001, pp. 245-256
6. Nguyen-Vu, PA; Fackler, I; Rust, A; DeClue, JE; Sander, CA; Volkenandt, M; Flaig, M; Yeung, RS; Wienecke, R
   Loss of tuberin, the tuberous-sclerosis-complex-2 gene product is associated with angiogenesis
   JOURNAL OF CUTANEOUS PATHOLOGY
   
   P.A. Nguyen-Vu et al., "Loss of tuberin, the tuberous-sclerosis-complex-2 gene product is associated with angiogenesis", J CUT PATH, 28(9), 2001, pp. 470-475
7. Kito, M; Yabuta, K; Kato, S; Osawa, M; Okuda, H
   Gelastic seizures in clusters in a case of West syndrome after perinatal hypothalamic hemorrhage
   JOURNAL OF PERINATAL MEDICINE
   
   M. Kito et al., "Gelastic seizures in clusters in a case of West syndrome after perinatal hypothalamic hemorrhage", J PERIN MED, 29(4), 2001, pp. 357-359
8. Mortele, KJ; Ros, PR
   Cystic focal liver lesions in the adult: Differential CT and MR imaging features
   RADIOGRAPHICS
   
   K.J. Mortele e P.R. Ros, "Cystic focal liver lesions in the adult: Differential CT and MR imaging features", RADIOGRAPHI, 21(4), 2001, pp. 895-910
9. Dahan, H; Arrive, L; Wendum, D; le Pointe, HD; Djouhri, H; Tubiana, JM
   Retrorectal developmental cysts in adults: Clinical and radiologic-histopathologic review, differential diagnosis, and treatment
   RADIOGRAPHICS
   
   H. Dahan et al., "Retrorectal developmental cysts in adults: Clinical and radiologic-histopathologic review, differential diagnosis, and treatment", RADIOGRAPHI, 21(3), 2001, pp. 575-584
10. Liu, F; Chau, KY; Arlotta, P; Ono, SJ
    The HMG I proteins - Dynamic roles in gene activation, development, and tumorigenesis
    IMMUNOLOGIC RESEARCH
    
    F. Liu et al., "The HMG I proteins - Dynamic roles in gene activation, development, and tumorigenesis", IMMUNOL RES, 24(1), 2001, pp. 13-29
11. Eder, HG; Leber, KA; Eustacchio, S; Pendl, G
    The role of gamma knife radiosurgery in children
    CHILDS NERVOUS SYSTEM
    
    H.G. Eder et al., "The role of gamma knife radiosurgery in children", CHILD NERV, 17(6), 2001, pp. 341-346
12. Rogalla, P; Blank, C; Helbig, R; Wosniok, W; Bullerdiek, J
    Significant correlation between the breakpoints of rare clonal aberrationsin benign solid tumors and the assignment of HMGIY retropseudogenes
    CANCER GENETICS AND CYTOGENETICS
    
    P. Rogalla et al., "Significant correlation between the breakpoints of rare clonal aberrationsin benign solid tumors and the assignment of HMGIY retropseudogenes", CANC GENET, 130(1), 2001, pp. 51-56
13. Lemke, I; Rogalla, P; Bullerdiek, J
    Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27 similar to q28;q14 similar to q15) in a lipoma
    CANCER GENETICS AND CYTOGENETICS
    
    I. Lemke et al., "Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27 similar to q28;q14 similar to q15) in a lipoma", CANC GENET, 129(2), 2001, pp. 161-164
14. Delalande, O; Rodriguez, D; Chiron, C; Fohlen, M
    Successful surgical relief of seizures associated with hamartoma of the floor of the fourth ventricle in children: Report of two cases
    NEUROSURGERY
    
    O. Delalande et al., "Successful surgical relief of seizures associated with hamartoma of the floor of the fourth ventricle in children: Report of two cases", NEUROSURGER, 49(3), 2001, pp. 726-730
15. Piekielko, A; Drung, A; Rogalla, P; Schwanbeck, R; Heyduk, T; Gerharz, M; Bullerdiek, J; Wisniewski, JR
    Distinct organization of DNA complexes of various HMGI/Y family proteins and their modulation upon mitotic phosphorylation
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    A. Piekielko et al., "Distinct organization of DNA complexes of various HMGI/Y family proteins and their modulation upon mitotic phosphorylation", J BIOL CHEM, 276(3), 2001, pp. 1984-1992
16. Dabora, SL; Jozwiak, S; Franz, DN; Roberts, PS; Nieto, A; Chung, J; Choy, YS; Reeve, MP; Thiele, E; Egelhoff, JC; Kasprzyk-Obara, J; Domanska-Pakiela, D; Kwiatkowski, DJ
    Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    S.L. Dabora et al., "Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs", AM J HU GEN, 68(1), 2001, pp. 64-80
17. Wisniewski, JR; Schwanbeck, R
    High mobility group I/Y: Multifunctional chromosomal proteins causally involved in tumor progression and malignant transformation (Review)
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    
    J.R. Wisniewski e R. Schwanbeck, "High mobility group I/Y: Multifunctional chromosomal proteins causally involved in tumor progression and malignant transformation (Review)", INT J MOL M, 6(4), 2000, pp. 409-419
18. Garcia, A; Gutierrez, MA; Barrasa, J; Herranz, JL
    Cryptogenic gelastic epilepsy of frontal lobe origin: A paediatric case report
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    
    A. Garcia et al., "Cryptogenic gelastic epilepsy of frontal lobe origin: A paediatric case report", SEIZURE-E J, 9(4), 2000, pp. 297-300
19. Likavec, AM; Dickerman, RD; Heiss, JD; Liow, K
    Retrospective analysis of surgical treatment outcomes for gelastic seizures: a review of the literature
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    
    A.M. Likavec et al., "Retrospective analysis of surgical treatment outcomes for gelastic seizures: a review of the literature", SEIZURE-E J, 9(3), 2000, pp. 204-207
20. Lefton, DR; Pinto, RS; Silvera, VM; DeLara, FA; Schwartz, JB; Haller, JO
    Radiologic features of pediatric thalamic and hypothalamic tumors
    CRITICAL REVIEWS IN DIAGNOSTIC IMAGING
    
    D.R. Lefton et al., "Radiologic features of pediatric thalamic and hypothalamic tumors", CR R DIAGN, 41(4), 2000, pp. 237-278
21. So, EL; O'Brien, TJ; Brinkmann, BH; Mullan, BP
    The EEG evaluation of single photon emission computed tomography abnormalities in epilepsy
    JOURNAL OF CLINICAL NEUROPHYSIOLOGY
    
    E.L. So et al., "The EEG evaluation of single photon emission computed tomography abnormalities in epilepsy", J CL NEURPH, 17(1), 2000, pp. 10-28
22. Murthy, V; Haddad, LA; Smith, N; Pinney, D; Tyszkowski, R; Brown, D; Ramesh, V
    Similarities and differences in the subcellular localization of hamartin and tuberin in the kidney
    AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    
    V. Murthy et al., "Similarities and differences in the subcellular localization of hamartin and tuberin in the kidney", AM J P-REN, 278(5), 2000, pp. F737-F746
23. Parry, L; Maynard, JH; Patel, A; Hodges, AK; von Deimling, A; Sampson, JR; Cheadle, JP
    Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours
    HUMAN GENETICS
    
    L. Parry et al., "Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours", HUM GENET, 107(4), 2000, pp. 350-356
24. Kutsche, K; Glauner, E; Knauf, S; Pomarino, A; Schmidt, M; Schroder, B; Nothwang, HG; Schuler, HM; Goecke, TO; Kersten, AJ; Althaus, C; Gal, A
    Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium
    CYTOGENETICS AND CELL GENETICS
    
    K. Kutsche et al., "Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium", CYTOG C GEN, 91(1-4), 2000, pp. 141-147
25. Duniho, S; Schulman, FY; Morrison, A; Mena, H; Koestner, A
    A subependymal giant cell astrocytoma in a cat
    VETERINARY PATHOLOGY
    
    S. Duniho et al., "A subependymal giant cell astrocytoma in a cat", VET PATH, 37(3), 2000, pp. 275-278
26. Engelborghs, S; D'Hooge, R; De Deyn, PP
    Pathophysiology of epilepsy
    ACTA NEUROLOGICA BELGICA
    
    S. Engelborghs et al., "Pathophysiology of epilepsy", ACT NEUR BE, 100(4), 2000, pp. 201-213
27. Arai, Y; Ackerley, CA; Becker, LE
    Tuberin expression in ganglioglioma
    ULTRASTRUCTURAL PATHOLOGY
    
    Y. Arai et al., "Tuberin expression in ganglioglioma", ULTRA PATH, 24(2), 2000, pp. 93-98
28. Becker, AE
    Primary heart tumors in the pediatric age group: A review of salient pathologic features relevant for clinicians
    PEDIATRIC CARDIOLOGY
    
    A.E. Becker, "Primary heart tumors in the pediatric age group: A review of salient pathologic features relevant for clinicians", PEDIAT CARD, 21(4), 2000, pp. 317-323
29. Sener, RN
    Septum pellucidum hamartomas in neurofibromatosis type 1
    JOURNAL OF NEURORADIOLOGY
    
    R.N. Sener, "Septum pellucidum hamartomas in neurofibromatosis type 1", J NEURORAD, 27(1), 2000, pp. 19-23
30. Schilke, K; Schaefer, F; Waldherr, R; Rohrschneider, W; John, C; Himbert, U; Mayatepek, E; Tariverdian, G
    A case of Perlman syndrome: Fetal gigantism, renal dysplasia, and severe neurological deficits
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    K. Schilke et al., "A case of Perlman syndrome: Fetal gigantism, renal dysplasia, and severe neurological deficits", AM J MED G, 91(1), 2000, pp. 29-33
31. Regis, J; Bartolomei, F; de Toffol, B; Genton, P; Kobayashi, T; Mori, Y; Takakura, K; Hori, T; Inoue, H; Schrottner, O; Pendl, G; Wolf, A; Arita, K; Chauvel, P
    Gamma knife surgery for epilepsy related to hypothalamic hamartomas
    NEUROSURGERY
    
    J. Regis et al., "Gamma knife surgery for epilepsy related to hypothalamic hamartomas", NEUROSURGER, 47(6), 2000, pp. 1343-1351
32. Jain, D; Sarode, VR; Abdul-Karim, FW; Homer, R; Robert, ME
    Evidence for the neoplastic transformation of Von-Meyenburg complexes
    AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    
    D. Jain et al., "Evidence for the neoplastic transformation of Von-Meyenburg complexes", AM J SURG P, 24(8), 2000, pp. 1131-1139
33. Van Poppel, H; Nilsson, S; Algaba, F; Bergerheim, U; Dal Cin, P; Fleming, S; Hellsten, S; Kirkali, Z; Klotz, L; Lindblad, P; Ljungberg, B; Mulders, P; Roskams, T; Ross, RK; Walker, C; Wersail, P
    Precancerous lesions in the kidney
    SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY
    
    H. Van Poppel et al., "Precancerous lesions in the kidney", SC J UROL N, 34, 2000, pp. 136-165
34. von Barany, RU; Thiel, A; Erlemann, R
    Unclear retroperitoneal and intrahepatic masses
    RADIOLOGE
    
    R.U. von Barany et al., "Unclear retroperitoneal and intrahepatic masses", RADIOLOGE, 40(3), 2000, pp. 321-323
35. Gomez-Anson, B; Thom, M; Moran, N; Stevens, J; Scaravilli, F
    Imaging and radiological-pathological correlation in histologically provencases of focal cortical dysplasia and other glial and neuronoglial malformative lesions in adults
    NEURORADIOLOGY
    
    B. Gomez-Anson et al., "Imaging and radiological-pathological correlation in histologically provencases of focal cortical dysplasia and other glial and neuronoglial malformative lesions in adults", NEURORADIOL, 42(3), 2000, pp. 157-167
36. Zaatreh, M; Tennison, M; Greenwood, RS
    Successful treatment of hypothalamic seizures and precocious puberty with GnRH analogue
    NEUROLOGY
    
    M. Zaatreh et al., "Successful treatment of hypothalamic seizures and precocious puberty with GnRH analogue", NEUROLOGY, 55(12), 2000, pp. 1908-1910
37. Chen, MT; Yeong, EK; Horng, SY
    Intralesional corticosteroid therapy in proliferating head and neck hemangiomas: A review of 155 cases
    JOURNAL OF PEDIATRIC SURGERY
    
    M.T. Chen et al., "Intralesional corticosteroid therapy in proliferating head and neck hemangiomas: A review of 155 cases", J PED SURG, 35(3), 2000, pp. 420-423
38. Mizuguchi, M; Takashima, S; Yamanouchi, H; Nakazato, Y; Mitani, H; Hino, O
    Novel cerebral lesions in the Eker rat model of tuberous sclerosis: Cortical tuber and anaplastic ganglioglioma
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    
    M. Mizuguchi et al., "Novel cerebral lesions in the Eker rat model of tuberous sclerosis: Cortical tuber and anaplastic ganglioglioma", J NE EXP NE, 59(3), 2000, pp. 188-196
39. So, EL
    Integration of EEG, MRI, and SPECT in localizing the seizure focus for epilepsy surgery
    EPILEPSIA
    
    E.L. So, "Integration of EEG, MRI, and SPECT in localizing the seizure focus for epilepsy surgery", EPILEPSIA, 41, 2000, pp. S48-S54
40. Hennessy, MJ; Elwes, RDC; Binnie, CD; Polkey, CE
    Failed surgery for epilepsy - A study of persistence and recurrence of seizures following temporal resection
    BRAIN
    
    M.J. Hennessy et al., "Failed surgery for epilepsy - A study of persistence and recurrence of seizures following temporal resection", BRAIN, 123, 2000, pp. 2445-2466
41. Schwanbeck, R; Gerharz, M; Drung, A; Rogalla, P; Piekielko, A; Blank, C; Bullerdiek, J; Wisniewski, JR
    Point mutations within AT-hook domains of the HMGI homologue HMGIYL1 affect binding to gene promoter but not to four-way junction DNA
    BIOCHEMISTRY
    
    R. Schwanbeck et al., "Point mutations within AT-hook domains of the HMGI homologue HMGIYL1 affect binding to gene promoter but not to four-way junction DNA", BIOCHEM, 39(47), 2000, pp. 14419-14425
42. Hyman, MH; Whittemore, VH
    National Institutes of Health consensus conference: Tuberous sclerosis complex
    ARCHIVES OF NEUROLOGY
    
    M.H. Hyman e V.H. Whittemore, "National Institutes of Health consensus conference: Tuberous sclerosis complex", ARCH NEUROL, 57(5), 2000, pp. 662-665
43. Zhang, H; Nanba, E; Yamamoto, T; Ninomiya, H; Ohno, K; Mizuguchi, M; Takeshita, K
    Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
    JOURNAL OF HUMAN GENETICS
    
    H. Zhang et al., "Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex", J HUM GENET, 44(6), 1999, pp. 391-396
44. Takemura, T; Kusafuka, K; Fujiwara, M; Masuda, R; Furuhata, Y; Tanaka, I; Inoue, M
    An immunohistochemical study of the mesenchymal and epithelial components of pulmonary chondromatous hamartomas
    PATHOLOGY INTERNATIONAL
    
    T. Takemura et al., "An immunohistochemical study of the mesenchymal and epithelial components of pulmonary chondromatous hamartomas", PATHOL INT, 49(11), 1999, pp. 938-946
45. Biraben, A; Sartori, E; Taussig, D; Bernard, AM; Scarabin, JM
    Gelastic seizures: video-EEG and scintigraphic analysis of a case with a frontal focus review of the literature and pathophysiological hypotheses
    EPILEPTIC DISORDERS
    
    A. Biraben et al., "Gelastic seizures: video-EEG and scintigraphic analysis of a case with a frontal focus review of the literature and pathophysiological hypotheses", EPILEPT DIS, 1(4), 1999, pp. 221-228
46. Duchowny, M
    Pediatric epilepsy surgery: the widening spectrum of surgical candidacy
    EPILEPTIC DISORDERS
    
    M. Duchowny, "Pediatric epilepsy surgery: the widening spectrum of surgical candidacy", EPILEPT DIS, 1(3), 1999, pp. 143-151
47. Tallini, G; Dal Cin, P
    HMGI(Y) and HMGI-C dysregulation: A common occurrence in human tumors
    ADVANCES IN ANATOMIC PATHOLOGY
    
    G. Tallini e P. Dal Cin, "HMGI(Y) and HMGI-C dysregulation: A common occurrence in human tumors", ADV ANAT PA, 6(5), 1999, pp. 237-246
48. Niida, Y; Lawrence-Smith, N; Banwell, A; Hammer, E; Lewis, J; Beauchamp, RL; Sims, K; Ramesh, VL; Ozelius, L
    Analysis of both TCS1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis
    HUMAN MUTATION
    
    Y. Niida et al., "Analysis of both TCS1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis", HUM MUTAT, 14(5), 1999, pp. 412-422
49. Semelka, RC; Hussain, SM; Marcos, HB; Woosley, JT
    Biliary hamartomas: Solitary and multiple lesions shown on current MR techniques including gadolinium enhancement
    JMRI-JOURNAL OF MAGNETIC RESONANCE IMAGING
    
    R.C. Semelka et al., "Biliary hamartomas: Solitary and multiple lesions shown on current MR techniques including gadolinium enhancement", J MAGN R I, 10(2), 1999, pp. 196-201
50. Gattas, GJF; Quade, BJ; Nowak, RA; Morton, CC
    HMGIC expression in human adult and fetal tissues and in uterine leiomyomata
    GENES CHROMOSOMES & CANCER
    
    G.J.F. Gattas et al., "HMGIC expression in human adult and fetal tissues and in uterine leiomyomata", GENE CHROM, 25(4), 1999, pp. 316-322
51. Regis, J; Bartolomei, F; Metellus, P; Rey, M; Genton, P; Dravet, C; Bureau, M; Semah, F; Gastaut, JL; Peragut, JC; Chauvel, P
    Radiosurgery for trigeminal neuralgia and epilepsy
    NEUROSURGERY CLINICS OF NORTH AMERICA
    
    J. Regis et al., "Radiosurgery for trigeminal neuralgia and epilepsy", NEUROSURG C, 10(2), 1999, pp. 359
52. Johnson, MW; Emelin, JK; Park, SH; Vinters, HV
    Co-localization of TSC1 and TSG2 gene products in tubers of patients with tuberous sclerosis
    BRAIN PATHOLOGY
    
    M.W. Johnson et al., "Co-localization of TSC1 and TSG2 gene products in tubers of patients with tuberous sclerosis", BRAIN PATH, 9(1), 1999, pp. 45-54
53. Maher, MM; Dervan, P; Keogh, B; Murray, JG
    Bile duct hamartomas (Von Meyenburg complexes): value of MR imaging in diagnosis
    ABDOMINAL IMAGING
    
    M.M. Maher et al., "Bile duct hamartomas (Von Meyenburg complexes): value of MR imaging in diagnosis", ABDOM IMAG, 24(2), 1999, pp. 171-173
54. Mendez, MF; Nakawatase, TV; Brown, CV
    Involuntary laughter and inappropriate hilarity
    JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
    
    M.F. Mendez et al., "Involuntary laughter and inappropriate hilarity", J NEUROP CL, 11(2), 1999, pp. 253-258
55. Potente, G; Macori, F; Caimi, M; Mingazzini, P; Volpino, P
    Noncalcified pulmonary hamartomas: Computed tomography enhancement patterns with histologic correlation
    JOURNAL OF THORACIC IMAGING
    
    G. Potente et al., "Noncalcified pulmonary hamartomas: Computed tomography enhancement patterns with histologic correlation", J THOR IMAG, 14(2), 1999, pp. 101-104
56. Toyoshima, M; Ohno, K; Katsumoto, T; Maki, H; Takeshita, K
    Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis
    BRAIN & DEVELOPMENT
    
    M. Toyoshima et al., "Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis", BRAIN DEVEL, 21(3), 1999, pp. 184-191
57. Chiacchio, R; Panico, L; D'Antonio, A; Delrio, P; Bifano, D; Avallone, M; Pettinato, G
    Mammary hamartomas: An immunohistochemical study of ten cases
    PATHOLOGY RESEARCH AND PRACTICE
    
    R. Chiacchio et al., "Mammary hamartomas: An immunohistochemical study of ten cases", PATH RES PR, 195(4), 1999, pp. 231-236
58. Rocken, C; Schneider-Stock, R; Buhtz, P; Manger, T; Roessner, A
    Hepatic angiomyolipoma in a 26-year-old Caucasian woman with a history of tibial osteosarcoma
    PATHOLOGY RESEARCH AND PRACTICE
    
    C. Rocken et al., "Hepatic angiomyolipoma in a 26-year-old Caucasian woman with a history of tibial osteosarcoma", PATH RES PR, 195(11), 1999, pp. 765-772
59. Beltramello, A; Puppini, G; Bricolo, A; Andreis, IAB; El-Dalati, G; Longa, L; Polidoro, S; Zavarise, G; Marradi, P
    Does the tuberous sclerosis complex include intracranial aneurysms? A casereport with a review of the literature
    PEDIATRIC RADIOLOGY
    
    A. Beltramello et al., "Does the tuberous sclerosis complex include intracranial aneurysms? A casereport with a review of the literature", PEDIAT RAD, 29(3), 1999, pp. 206-211
60. Bullerdiek, J; Rommel, B
    Diagnostic and molecular implications of specific chromosomal translocations in mesenchymal tumors
    HISTOLOGY AND HISTOPATHOLOGY
    
    J. Bullerdiek e B. Rommel, "Diagnostic and molecular implications of specific chromosomal translocations in mesenchymal tumors", HIST HISTOP, 14(4), 1999, pp. 1165-1173
61. Tong, JT; Bateman, JB
    Selective B-wave reduction with congenital cataract in neurofibromatosis-2
    OPHTHALMOLOGY
    
    J.T. Tong e J.B. Bateman, "Selective B-wave reduction with congenital cataract in neurofibromatosis-2", OPHTHALMOL, 106(9), 1999, pp. 1681-1683
62. Henneveld, HT; van Lingen, RA; Hamel, BCJ; Stolte-Dijkstra, I; van Essen, AJ
    Perlman syndrome: Four additional cases and review
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    H.T. Henneveld et al., "Perlman syndrome: Four additional cases and review", AM J MED G, 86(5), 1999, pp. 439-446
63. Kattar, MM; Grignon, DJ; Eble, JN; Hurley, PM; Lewis, PE; Sakr, WE; Cher, ML
    Chromosomal analysis of renal angiomyolipoma by comparative genomic hybridization: Evidence for clonal origin
    HUMAN PATHOLOGY
    
    M.M. Kattar et al., "Chromosomal analysis of renal angiomyolipoma by comparative genomic hybridization: Evidence for clonal origin", HUMAN PATH, 30(3), 1999, pp. 295-299
64. Westerman, AM; Wilson, JHP
    Peutz-Jeghers syndrome: Risks of a hereditary condition - A clinical review
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    
    A.M. Westerman e J.H.P. Wilson, "Peutz-Jeghers syndrome: Risks of a hereditary condition - A clinical review", SC J GASTR, 34, 1999, pp. 64-70
65. Manjunath, S; Hock, YL; Cunnington, AR
    A rare but important cause of focal hepatic lesions - von Meyenburg complexes or bile duct microhamartomas.
    POSTGRADUATE MEDICAL JOURNAL
    
    S. Manjunath et al., "A rare but important cause of focal hepatic lesions - von Meyenburg complexes or bile duct microhamartomas.", POSTG MED J, 75(887), 1999, pp. 567-568
66. Kwiatkowska, J; Wigowska-Sowinska, J; Napierala, D; Slomski, R; Kwiatkowski, DJ
    Mosaicism in tuberous sclerosis as a potential cause of the failure of molecular diagnosis
    NEW ENGLAND JOURNAL OF MEDICINE
    
    J. Kwiatkowska et al., "Mosaicism in tuberous sclerosis as a potential cause of the failure of molecular diagnosis", N ENG J MED, 340(9), 1999, pp. 703-707
67. Onda, H; Lueck, A; Marks, PW; Warren, HB; Kwiatkowski, DJ
    Tsc2(+/-) mice develop tumors in multiple sites that express gelsolin and are influenced by genetic background
    JOURNAL OF CLINICAL INVESTIGATION
    
    H. Onda et al., "Tsc2(+/-) mice develop tumors in multiple sites that express gelsolin and are influenced by genetic background", J CLIN INV, 104(6), 1999, pp. 687-695
68. Martin, ES; Pelaez, JMF; Meiroso, BV; Fuentes, PMD; Hernandez, MIS; Mendez, LS
    Asymptomatic abdominal mass
    REVISTA CLINICA ESPANOLA
    
    E.S. Martin et al., "Asymptomatic abdominal mass", REV CLIN ES, 199(8), 1999, pp. 535-536
69. Striano, S; Meo, R; Bilo, L; Cirillo, S; Nocerino, C; Ruosi, P; Striano, P; Estraneo, A
    Gelastic epilepsy: Symptomatic and cryptogenic cases
    EPILEPSIA
    
    S. Striano et al., "Gelastic epilepsy: Symptomatic and cryptogenic cases", EPILEPSIA, 40(3), 1999, pp. 294-302
70. Jiang, CY; Esufali, S; Berk, T; Gallinger, S; Cohen, Z; Tobi, M; Redston, M; Bapat, B
    STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients
    CLINICAL GENETICS
    
    C.Y. Jiang et al., "STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients", CLIN GENET, 56(2), 1999, pp. 136-141
71. Battista, S; Fidanza, V; Fedele, M; Klein-Szanto, AJP; Outwater, E; Brunner, H; Santoro, M; Croce, CM; Fusco, A
    The expression of a truncated HMGI-C gene induces gigantism associated with lipomatosis
    CANCER RESEARCH
    
    S. Battista et al., "The expression of a truncated HMGI-C gene induces gigantism associated with lipomatosis", CANCER RES, 59(19), 1999, pp. 4793-4797
72. Kiryu, T; Kawaguchi, S; Matsui, E; Hoshi, H; Kokubo, M; Shimokawa, K
    Multiple chondromatous hamartomas of the lung - A case report and review of the literature with special reference to Carney syndrome
    CANCER
    
    T. Kiryu et al., "Multiple chondromatous hamartomas of the lung - A case report and review of the literature with special reference to Carney syndrome", CANCER, 85(12), 1999, pp. 2557-2561
73. Au, KS; Hebert, AA; Roach, ES; Northrup, H
    Complete inactivation of the TSC2 gene leads to formation of hamartomas
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    K.S. Au et al., "Complete inactivation of the TSC2 gene leads to formation of hamartomas", AM J HU GEN, 65(6), 1999, pp. 1790-1795
74. YOUNG J; POVEY S
    THE GENETIC-BASIS OF TUBEROUS SCLEROSIS
    Molecular medicine today
    
    J. Young e S. Povey, "THE GENETIC-BASIS OF TUBEROUS SCLEROSIS", Molecular medicine today, 4(7), 1998, pp. 313-319
75. SHEHATA BM; PATTERSON K; THOMAS JE; SCALABARNETT D; DASU S; ROBINSON HB
    HISTIOCYTOID CARDIOMYOPATHY - 3 NEW CASES AND A REVIEW OF THE LITERATURE
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    
    B.M. Shehata et al., "HISTIOCYTOID CARDIOMYOPATHY - 3 NEW CASES AND A REVIEW OF THE LITERATURE", PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 1(1), 1998, pp. 56-69
76. ZHONG PQ; ZHI FX; LI R; XUE JL; SHU GY
    LONG-TERM RESULTS OF INTRATUMOROUS BLEOMYCIN-A5 INJECTION FOR HEAD AND NECK LYMPHANGIOMA
    Oral surgery, oral medicine, oral pathology, oral radiology and endodontics
    
    P.Q. Zhong et al., "LONG-TERM RESULTS OF INTRATUMOROUS BLEOMYCIN-A5 INJECTION FOR HEAD AND NECK LYMPHANGIOMA", Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 86(2), 1998, pp. 139-144
77. GEORGAKOULIAS N; VIZE C; JENKINS A; SINGOUNAS E
    HYPOTHALAMIC HAMARTOMAS CAUSING GELASTIC EPILEPSY - 2 CASES AND A REVIEW OF THE LITERATURE
    Seizure
    
    N. Georgakoulias et al., "HYPOTHALAMIC HAMARTOMAS CAUSING GELASTIC EPILEPSY - 2 CASES AND A REVIEW OF THE LITERATURE", Seizure, 7(2), 1998, pp. 167-171
78. KAZMIERCZAK B; DALCIN P; WANSCHURA S; BORRMANN L; FUSCO A; VANDENBERGHE H; BULLERDIEK J
    HMGIY IS THE TARGET OF 6P21.3 REARRANGEMENTS IN VARIOUS BENIGN MESENCHYMAL TUMORS
    Genes chromosomes & cancer (Print)
    
    B. Kazmierczak et al., "HMGIY IS THE TARGET OF 6P21.3 REARRANGEMENTS IN VARIOUS BENIGN MESENCHYMAL TUMORS", Genes chromosomes & cancer (Print), 23(4), 1998, pp. 279-285
79. PEDEUTOUR F; QUADE BJ; WEREMOWICZ S; DALCIN P; ALI S; MORTON CC
    LOCALIZATION AND EXPRESSION OF THE HUMAN ESTROGEN-RECEPTOR BETA-GENE IN UTERINE LEIOMYOMATA
    Genes chromosomes & cancer (Print)
    
    F. Pedeutour et al., "LOCALIZATION AND EXPRESSION OF THE HUMAN ESTROGEN-RECEPTOR BETA-GENE IN UTERINE LEIOMYOMATA", Genes chromosomes & cancer (Print), 23(4), 1998, pp. 361-366
80. ROGALLA P; KAZMIERCZAK B; MEYERBOLTE K; TRAN KH; BULLERDIEK J
    THE T(3-12)(Q27-Q14-Q15) WITH UNDERLYING HMGIC-LPP FUSION IS NOT DETERMINING AN ADIPOCYTIC PHENOTYPE
    Genes, chromosomes & cancer
    
    P. Rogalla et al., "THE T(3-12)(Q27-Q14-Q15) WITH UNDERLYING HMGIC-LPP FUSION IS NOT DETERMINING AN ADIPOCYTIC PHENOTYPE", Genes, chromosomes & cancer, 22(2), 1998, pp. 100-104
81. BRADSHAW N; BREWER C; FITZPATRICK D; MURRAY G; RODGERS F; PORTEOUS M; CAMPBELL H
    GUIDELINES AND CARE PATHWAYS FOR GENETIC-DISEASES - THE SCOTTISH COLLABORATIVE PROJECT ON TUBEROUS SCLEROSIS
    European journal of human genetics
    
    N. Bradshaw et al., "GUIDELINES AND CARE PATHWAYS FOR GENETIC-DISEASES - THE SCOTTISH COLLABORATIVE PROJECT ON TUBEROUS SCLEROSIS", European journal of human genetics, 6(5), 1998, pp. 445-458
82. HAZIM W; MAUTNER VF; CHRISTIANI B; HAASE W
    DETECTION OF RETINAL CHANGES IN NEUROFIBROMATOSIS-2
    Der Ophthalmologe
    
    W. Hazim et al., "DETECTION OF RETINAL CHANGES IN NEUROFIBROMATOSIS-2", Der Ophthalmologe, 95(10), 1998, pp. 687-690
83. Wohlgemuth, WA; Bottger, J; Bohndorf, K
    MRI, CT, US and ERCP in the evaluation of bile duet hamartomas (von Meyenburg complex): a case report
    EUROPEAN RADIOLOGY
    
    W.A. Wohlgemuth et al., "MRI, CT, US and ERCP in the evaluation of bile duet hamartomas (von Meyenburg complex): a case report", EUR RADIOL, 8(9), 1998, pp. 1623-1626
84. LYNCH RA; PIPER M; BANKIER A; BHUGRA B; SURTI U; LIU J; BUCKLER A; DEAR PH; MENON AG
    GENOMIC AND FUNCTIONAL MAP OF THE CHROMOSOME-14 T(12-14) BREAKPOINT CLUSTER REGION IN UTERINE LEIOMYOMA
    Genomics (San Diego, Calif.)
    
    R.A. Lynch et al., "GENOMIC AND FUNCTIONAL MAP OF THE CHROMOSOME-14 T(12-14) BREAKPOINT CLUSTER REGION IN UTERINE LEIOMYOMA", Genomics (San Diego, Calif.), 52(1), 1998, pp. 17-26
85. Roach, ES; Gomez, MR; Northrup, H
    Tuberous sclerosis complex consensus conference: Revised clinical diagnostic criteria
    JOURNAL OF CHILD NEUROLOGY
    
    E.S. Roach et al., "Tuberous sclerosis complex consensus conference: Revised clinical diagnostic criteria", J CHILD NEU, 13(12), 1998, pp. 624-628
86. LUO TY; ITAI Y; EGUCHI N; KUROSAKI Y; ONAYA H; AHMADI T; NIITSU M; TSUNODA HS
    VON-MEYENBURG COMPLEXES OF THE LIVER - IMAGING FINDINGS
    Journal of computer assisted tomography
    
    T.Y. Luo et al., "VON-MEYENBURG COMPLEXES OF THE LIVER - IMAGING FINDINGS", Journal of computer assisted tomography, 22(3), 1998, pp. 372-378
87. BHUGRA B; SMOLAREK TA; LYNCH RA; MELONI AM; SANDBERG AA; DEAVEN L; MENON AG
    CLONING OF A BREAKPOINT CLUSTER REGION ON CHROMOSOME-14 IN UTERINE LEIOMYOMA
    Cancer letters
    
    B. Bhugra et al., "CLONING OF A BREAKPOINT CLUSTER REGION ON CHROMOSOME-14 IN UTERINE LEIOMYOMA", Cancer letters, 126(2), 1998, pp. 119-126
88. FAHMY J; KAMINSKY CK; PARISI MT
    PERLMAN-SYNDROME - A CASE-REPORT EMPHASIZING ITS SIMILARITY TO AND DISTINCTION FROM BECKWITH-WIEDEMANN AND PRUNE-BELLY SYNDROMES
    Pediatric radiology
    
    J. Fahmy et al., "PERLMAN-SYNDROME - A CASE-REPORT EMPHASIZING ITS SIMILARITY TO AND DISTINCTION FROM BECKWITH-WIEDEMANN AND PRUNE-BELLY SYNDROMES", Pediatric radiology, 28(3), 1998, pp. 179-182
89. Rogalla, P; Borda, Z; Meyer-Bolte, K; Tran, KH; Hauke, S; Nimzyk, R; Bullerdiek, J
    Mapping and molecular characterization of five HMG1-related DNA sequences
    CYTOGENETICS AND CELL GENETICS
    
    P. Rogalla et al., "Mapping and molecular characterization of five HMG1-related DNA sequences", CYTOG C GEN, 83(1-2), 1998, pp. 124-129
90. UEBING A; STIEH J; JUNG O; KRAMER HH; OLDIGS HD
    ATRIAL ECTOPIC TACHYCARDIA IN AN INFANT C AUSED BY A TUMOR IN THE INTERATRIAL SEPTUM
    Zeitschrift fur Kardiologie
    
    A. Uebing et al., "ATRIAL ECTOPIC TACHYCARDIA IN AN INFANT C AUSED BY A TUMOR IN THE INTERATRIAL SEPTUM", Zeitschrift fur Kardiologie, 87(6), 1998, pp. 478-481
91. MEYER CA; WHITE CS
    CARTILAGINOUS DISORDERS OF THE CHEST
    Radiographics
    
    C.A. Meyer e C.S. White, "CARTILAGINOUS DISORDERS OF THE CHEST", Radiographics, 18(5), 1998, pp. 1109-1123
92. CHITTY LS; CLARK T; MAXWELL D
    PERLMAN-SYNDROME - A CAUSE OF ENLARGED, HYPERECHOGENIC KIDNEYS
    Prenatal diagnosis
    
    L.S. Chitty et al., "PERLMAN-SYNDROME - A CAUSE OF ENLARGED, HYPERECHOGENIC KIDNEYS", Prenatal diagnosis, 18(11), 1998, pp. 1163-1168
93. WALKER C
    MOLECULAR-GENETICS OF RENAL CARCINOGENESIS
    Toxicologic pathology
    
    C. Walker, "MOLECULAR-GENETICS OF RENAL CARCINOGENESIS", Toxicologic pathology, 26(1), 1998, pp. 113-120
94. MCKIBBIN M; AMOAKU W; BRADBURY JA
    INHERITED RETINAL TELANGIECTASIA WITH GLIAL PROLIFERATION
    Journal of pediatric ophthalmology and strabismus
    
    M. Mckibbin et al., "INHERITED RETINAL TELANGIECTASIA WITH GLIAL PROLIFERATION", Journal of pediatric ophthalmology and strabismus, 35(4), 1998, pp. 209-215
95. MARTIGNONI G; PEA M; BONETTI F; ZAMBONI G; CARBONARA C; LONGA L; ZANCANARO C; MARAN M; BRISIGOTTI M; MARIUZZI GM
    CARCINOMA-LIKE MONOTYPIC EPITHELIOID ANGIOMYOLIPOMA IN PATIENTS WITHOUT EVIDENCE OF TUBEROUS SCLEROSIS - A CLINICOPATHOLOGICAL AND GENETIC-STUDY
    The American journal of surgical pathology
    
    G. Martignoni et al., "CARCINOMA-LIKE MONOTYPIC EPITHELIOID ANGIOMYOLIPOMA IN PATIENTS WITHOUT EVIDENCE OF TUBEROUS SCLEROSIS - A CLINICOPATHOLOGICAL AND GENETIC-STUDY", The American journal of surgical pathology, 22(6), 1998, pp. 663-672
96. GUJRATI M; THOMAS C; ZELBY A; JENSEN E; LEE JM
    BANNAYAN-ZONANA-SYNDROME - A RARE AUTOSOMAL-DOMINANT SYNDROME WITH MULTIPLE LIPOMAS AND HEMANGIOMAS - A CASE-REPORT AND REVIEW OF LITERATURE
    Surgical neurology
    
    M. Gujrati et al., "BANNAYAN-ZONANA-SYNDROME - A RARE AUTOSOMAL-DOMINANT SYNDROME WITH MULTIPLE LIPOMAS AND HEMANGIOMAS - A CASE-REPORT AND REVIEW OF LITERATURE", Surgical neurology, 50(2), 1998, pp. 164-168
97. Rennebeck, G; Kleymenova, EV; Anderson, R; Yeung, RS; Artzt, K; Walker, CL
    Loss of function of the tuberous sclerosis 2 tumor suppressor gene resultsin embryonic lethality characterized by disrupted neuroepithelial growth and development
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    G. Rennebeck et al., "Loss of function of the tuberous sclerosis 2 tumor suppressor gene resultsin embryonic lethality characterized by disrupted neuroepithelial growth and development", P NAS US, 95(26), 1998, pp. 15629-15634
98. STEY CA; VOGT P; RUSSI EW
    ENDOBRONCHIAL LIPOMATOUS HAMARTOMA - A RARE CAUSE OF BRONCHIAL OCCLUSION
    Chest
    
    C.A. Stey et al., "ENDOBRONCHIAL LIPOMATOUS HAMARTOMA - A RARE CAUSE OF BRONCHIAL OCCLUSION", Chest, 113(1), 1998, pp. 254-255
99. CARETHERS JM; FURNARI FB; ZIGMAN AF; LAVINE JE; JONES MC; GRAHAM GE; TEEBI AS; HUANG HJS; HA HT; CHAUHAN DP; CHANG CL; CAVENEE WK; BOLAND CR
    ABSENCE OF PTEN MMAC1 GERM-LINE MUTATIONS IN SPORADIC BANNAYAN-RILEY-RUVALCABA-SYNDROME/
    Cancer research
    
    J.M. Carethers et al., "ABSENCE OF PTEN MMAC1 GERM-LINE MUTATIONS IN SPORADIC BANNAYAN-RILEY-RUVALCABA-SYNDROME/", Cancer research, 58(13), 1998, pp. 2724-2726
100. DELGADO R; BOJORGE BD; ALBORESSAAVEDRA J
     ATYPICAL ANGIOMYOLIPOMA OF THE KIDNEY - A DISTINCT MORPHOLOGIC VARIANT THAT IS EASILY CONFUSED WITH A VARIETY OF MALIGNANT NEOPLASMS
     Cancer
     
     R. Delgado et al., "ATYPICAL ANGIOMYOLIPOMA OF THE KIDNEY - A DISTINCT MORPHOLOGIC VARIANT THAT IS EASILY CONFUSED WITH A VARIETY OF MALIGNANT NEOPLASMS", Cancer, 83(8), 1998, pp. 1581-1592