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La ricerca find articoli where soggetti phrase all words 'HIRSCHSPRUNG DISEASE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 322 riferimenti
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    1. Black, FO; Pesznecker, SC; Allen, K; Gianna, C
      A vestibular phenotype for Waardenburg syndrome?

      OTOLOGY & NEUROTOLOGY
    2. Keating, JP; Frizelle, FA; Brasch, HD
      Low anterior resection and colonic J-pouch in the treatment of adult Hirschsprung's disease

      ANZ journal of surgery
    3. Machado, AF; Martin, LJ; Collins, MD
      Pax3 and the splotch mutations: Structure, function, and relationship to teratogenesis, including gene-chemical interactions

      CURRENT PHARMACEUTICAL DESIGN
    4. Nagahama, M; Semba, R; Tsuzuki, M; Ozaki, T
      Distribution of peripheral nerve terminals in the small and large intestine of congenital aganglionosis rats (Hirschsprung's disease rats)

      PATHOLOGY INTERNATIONAL
    5. Rajan, I; Gestblom, C; Kapur, RP
      RETMen2B-transgene produces sympathoadrenal tumors but does not prevent intestinal aganglionosis in gdnf-/- or gfr alpha-1-/- mice

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    6. Wegner, M
      Expression of transcription factors during oligodendroglial development

      MICROSCOPY RESEARCH AND TECHNIQUE
    7. Julies, MG; Moore, SW; Kotze, MJ; du Plessis, L
      Novel RET mutations in Hirschsprung's disease patients from the diverse South African population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    8. Kaariainen, H; Wallgren-Pettersson, C; Clarke, A; Pihko, H; Taskinen, H; Rintala, R
      Hirschsprung disease, mental retardation and dysmorphic facial features infive unrelated children

      CLINICAL DYSMORPHOLOGY
    9. Lore, F; Talidis, F; Di Cairano, G; Renieri, A
      Multiple endocrine neoplasia type 2 syndromes may be associated with renalmalformations

      JOURNAL OF INTERNAL MEDICINE
    10. Mercalli, E; Ghizzoni, S; Arighi, E; Alberti, L; Sangregorio, R; Radice, MT; Gishizky, ML; Pierotti, MA; Borrello, MG
      Key role of Shc signaling in the transforming pathway triggered by Ret/ptc2 oncoprotein

      ONCOGENE
    11. Gimm, O; Dziema, H; Brown, J; Cuong, HV; Hinze, R; Dralle, H; Mulligan, LM; Eng, C
      Over-representation of a germline variant in the gene encoding RET co-receptor GFR alpha-1 but not GFR alpha-2 or GFR alpha-3 in cases with sporadic medullary thyroid carcinoma

      ONCOGENE
    12. Dutton, KA; Pauliny, A; Lopes, SS; Elworthy, S; Carney, TJ; Rauch, J; Geisler, R; Haffter, P; Kelsh, RN
      Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates

      DEVELOPMENT
    13. Paratore, C; Goerich, DE; Suter, U; Wegner, M; Sommer, L
      Survival and glial fate acquisition of neural crest cells are regulated byan interplay between the transcription factor Sox10 and extrinsic combinatorial signaling

      DEVELOPMENT
    14. Martucciello, G; Favre, A; Torre, M; Prato, AP; Jasonni, V
      A new rapid acetylcholinesterase histochemical method for the intraoperative diagnosis of Hirschsprung's disease and intestinal neuronal dysplasia

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    15. Inoue, K; Shimotake, T; Tomiyama, H; Iwai, N
      Mutational analysis of the RET and GDNF gene in children with hypoganglionosis

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    16. Hunley, TE; Kon, V
      Update on endothelins - biology and clinical implications

      PEDIATRIC NEPHROLOGY
    17. Nirasawa, Y; Ito, Y; Fujiwara, T; Seki, N; Tanaka, H; Akagawa, K
      Altered immunoreactivity of HPC-1/syntaxin 1A in proliferated nerve fibersin the human aganglionic colon of Hirschsprung's disease

      JOURNAL OF MOLECULAR NEUROSCIENCE
    18. McCallion, AS; Chakravarti, A
      EDNRB/EDN3 and Hirschsprung disease Type II

      PIGMENT CELL RESEARCH
    19. de Graaff, E; Srinivas, S; Kilkenny, C; D'Agati, V; Mankoo, BS; Costantini, F; Pachnis, V
      Differential activities of the RET tyrosine kinase receptor isoforms during mammalian embryogenesis

      GENES & DEVELOPMENT
    20. Britsch, S; Goerich, DE; Riethmacher, D; Peirano, RI; Rossner, M; Nave, KA; Birchmeier, C; Wegner, M
      The transcription factor Sox10 is a key regulator of peripheral glial development

      GENES & DEVELOPMENT
    21. Zhou, B; Bae, SK; Malone, AC; Levinson, BB; Kuo, YM; Cilio, MR; Bertini, E; Hayflick, SJ; Gitschier, JM
      hGFR alpha-4: A new member of the GDNF receptor family and a candidate forNBIA

      PEDIATRIC NEUROLOGY
    22. van Kuyk, EM; Brugman-Boezeman, ATM; Wissink-Essink, M; Oerlemans, HM; Severijnen, RSVM; Bleijenberg, G
      Defecation problems in children with Hirschsprung's disease: a prospectivecontrolled study of a multidisciplinary behavioural treatment

      ACTA PAEDIATRICA
    23. Wiench, M; Wygoda, Z; Gubala, E; Wloch, J; Lisowska, K; Krassowski, J; Scieglinska, D; Fiszer-Kierzkowska, A; Lange, D; Kula, D; Zeman, M; Roskosz, J; Kukulska, A; Krawczyk, Z; Jarzab, B
      Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients

      JOURNAL OF CLINICAL ONCOLOGY
    24. Stratakis, CA
      Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    25. Sommer, L
      Context-dependent regulation of fate decisions in multipotent progenitor cells of the peripheral nervous system

      CELL AND TISSUE RESEARCH
    26. Dahia, PLM; Eng, C
      Hereditary endocrine neoplasias: Fundamental insights and the practice of clinical cancer genetics

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    27. Mulligan, LM
      Multiple endocrine neoplasia type 2: Molecular aspects

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    28. Ruiz, A; Antinolo, G; Fernandez, RM; Eng, C; Marcos, I; Borrego, S
      Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

      CLINICAL ENDOCRINOLOGY
    29. Mazziotti, MV; Langer, JC
      Laparoscopic full-thickness intestinal biopsies in children

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    30. Mograbi, B; Bocciardi, R; Bourget, I; Juhel, T; Farahi-Far, D; Romeo, G; Ceccherini, I; Rossi, B
      The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis

      MOLECULAR AND CELLULAR BIOLOGY
    31. Sock, E; Schmidt, K; Hermanns-Borgmeyer, I; Bosl, MR; Wegner, M
      Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8

      MOLECULAR AND CELLULAR BIOLOGY
    32. Haier, J; Nicolson, GL
      Cell biology and clinical implications of adhesion molecules in colorectaldiseases: Colorectal cancers, infections and inflammatory bowel diseases

      CLINICAL & EXPERIMENTAL METASTASIS
    33. Messineo, A; Codrich, D; Monai, M; Martellossi, S; Ventura, A
      The treatment of internal anal sphincter achalasia with botulinum toxin

      PEDIATRIC SURGERY INTERNATIONAL
    34. Chitnis, M; Chowdhary, S; Lazarus, C
      Application of the Malone antegrade continence enema principle in degenerative leiomyopathy

      PEDIATRIC SURGERY INTERNATIONAL
    35. Carvalho, JL; Campos, M; Soares-Oliveira, M; Estevao-Costa, J
      Laparoscopic colonic mapping of dysganglionosis

      PEDIATRIC SURGERY INTERNATIONAL
    36. Yoneda, A; Wang, Y; O'Briain, DS; Puri, P
      Cell-adhesion molecules and fibroblast growth factor signalling in Hirschsprung's disease

      PEDIATRIC SURGERY INTERNATIONAL
    37. Sidebotham, EL; Woodward, MN; Kenny, SE; Lloyd, DA; Vaillant, CR; Edgar, DH
      Assessment of protein gene product 9.5 as a marker of neural crest-derivedprecursor cells in the developing enteric nervous system

      PEDIATRIC SURGERY INTERNATIONAL
    38. Meyrat, BJ; Lesbros, Y; Laurini, RN
      Assessment of the colon innervation with serial biopsies above the aganglionic zone before the pull-through procedure in Hirschsprung's disease

      PEDIATRIC SURGERY INTERNATIONAL
    39. Demirbilek, S; Ozardalt, HI; Aydm, G
      Mast-cells distribution and colonic mucin composition in Hirschsprung's disease and intestinal neuronal dysplasia

      PEDIATRIC SURGERY INTERNATIONAL
    40. Nogueira, A; Campos, M; Soares-Oliveira, M; Estevao-Costa, J; Silva, P; Carneiro, F; Carvalho, JL
      Histochemical and immunohistochemical study of the intrinsic innervation in colonic dysganglionosis

      PEDIATRIC SURGERY INTERNATIONAL
    41. Wang, KS; Cahill, JL; Skarsgard, ED
      Omphalocele, colonic atresia, and Hirschsprung's disease: an unusual cluster of malformations in a single patient

      PEDIATRIC SURGERY INTERNATIONAL
    42. Manie, S; Santoro, M; Fusco, A; Billaud, M
      The RET receptor: function in development and dysfunction in congenital malformation

      TRENDS IN GENETICS
    43. Shanske, A; Ferreira, JC; Leonard, JC; Fuller, P; Marion, RW
      Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Marazita, ML; Maher, BS; Cooper, ME; Silvestri, JM; Huffman, AD; Smok-Pearsall, SM; Kowal, MH; Weese-Mayer, DE
      Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Weese-Mayer, DE; Silvestri, JM; Huffman, AD; Smok-Pearsall, SM; Kowal, MH; Maher, BS; Cooper, ME; Marazita, ML
      Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Katsanis, N; Ansley, SJ; Badano, JL; Eichers, ER; Lewis, RA; Hoskins, BE; Scambler, PJ; Davidson, WS; Beales, PL; Lupski, JR
      Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

      SCIENCE
    47. Smout, AJPM
      Manometry of the gastrointestinal tract: Toy or tool?

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    48. Gariepy, CE
      Intestinal motility disorders and development of the enteric nervous system

      PEDIATRIC RESEARCH
    49. Nakao, M; Suita, S; Taguchi, T; Hirose, R; Shima, Y
      Fourteen-year experience of acetylcholinesterase staining for rectal mucosal biopsy in neonatal Hirschsprung's disease

      JOURNAL OF PEDIATRIC SURGERY
    50. Prato, AP; Martucciello, G; Jasonni, V
      Solo-RBT: A new instrument for rectal suction biopsies in the diagnosis ofHirschsprung's disease

      JOURNAL OF PEDIATRIC SURGERY
    51. Rintala, RJ; Lindahl, H
      Sodium cromoglycate in the management of chronic or recurrent enterocolitis in patients with Hirschsprung's disease

      JOURNAL OF PEDIATRIC SURGERY
    52. Kubota, A; Yamauchi, K; Yonekura, T; Kosumi, T; Oyanagi, H; Mushiake, S; Nakayama, M; Imura, K; Okada, A
      Clinicopathologic relationship of hypoganglionosis

      JOURNAL OF PEDIATRIC SURGERY
    53. Hipolito, R; Haight, M; Dubois, J; Milstein, J; Goetzman, B
      Gastroschisis and Hirschsprung's disease: A rare combination

      JOURNAL OF PEDIATRIC SURGERY
    54. Boemers, TM; Bax, NMA; van Gool, JD
      The effect of rectosigmoidectomy and Duhamel-type pull-through procedure on lower urinary tract function in children with Hirschsprung's disease

      JOURNAL OF PEDIATRIC SURGERY
    55. Nemeth, L; Yoneda, A; Kader, M; Devaney, D; Puri, P
      Three-dimensional morphology of gut innervation in total intestinal aganglionosis using whole-mount preparation

      JOURNAL OF PEDIATRIC SURGERY
    56. Cheng, W; Au, DKK; Knowles, CH; Anand, P; Tam, PKH
      Hirschsprung's disease: A more generalised neuropathy?

      JOURNAL OF PEDIATRIC SURGERY
    57. Martin, MJ; Steele, SR; Noel, JM; Weichmann, D; Azarow, KS
      Total colonic manometry as a guide for surgical management of functional colonic obstruction: Preliminary results

      JOURNAL OF PEDIATRIC SURGERY
    58. Gao, Y; Li, GC; Zhang, XS; Xu, Q; Guo, ZT; Zheng, BJ; Li, P; Li, GW
      Primary transanal rectosigmoidectomy for Hirschsprung's disease: Preliminary results in the initial 33 cases

      JOURNAL OF PEDIATRIC SURGERY
    59. Facer, P; Knowles, CH; Tam, PKH; Ford, AP; Dyer, N; Baecker, PA; Anand, P
      Novel capsaicin (VR1) and purinergic (P2X(3)) receptors in Hirschsprung's intestine

      JOURNAL OF PEDIATRIC SURGERY
    60. Tomiyama, H; Shimotake, T; Ono, S; Kimura, O; Tokiwa, K; Iwai, N
      Relationship between the type of RET/GDNF/NTN or SOX10 gene mutations and long-term results after surgery for total colonic aganglionosis with small bowel involvement

      JOURNAL OF PEDIATRIC SURGERY
    61. Bahuau, M; Pelet, A; Vidaud, D; Lamireau, T; Le Bail, B; Munnich, A; Vidaud, M; Lyonnet, S; Lacombe, D
      GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotype

      JOURNAL OF MEDICAL GENETICS
    62. Boardman, JP; Syrris, P; Holder, SE; Robertson, NJ; Carter, N; Lakhoo, K
      A novel mutation in the endothelin B receptor gene in a patient with Shah-Waardenburg syndrome and Down syndrome

      JOURNAL OF MEDICAL GENETICS
    63. Amiel, J; Lyonnet, S
      Hirschsprung disease, associated syndromes, and genetics: a review

      JOURNAL OF MEDICAL GENETICS
    64. Gimm, O; Chi, HB; Dahia, PLM; Perren, A; Hinze, R; Komminoth, P; Dralle, H; Reynolds, PR; Eng, C
      Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    65. Anders, J; Kjaer, S; Ibanez, CF
      Molecular modeling of the extracellular domain of the RET receptor tyrosine kinase reveals multiple cadherin-like domains and a calcium-binding site

      JOURNAL OF BIOLOGICAL CHEMISTRY
    66. Sham, MH; Lui, VCH; Fu, M; Chen, B; Tam, PKH
      SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants

      GUT
    67. Gath, R; Goessling, A; Keller, KM; Koletzko, S; Coerdt, W; Muntefering, H; Wirth, S; Hofstra, RMW; Mulligan, L; Eng, C; von Deimling, A
      Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

      GUT
    68. Hanneman, MJG; Sprangers, MAG; De Mik, EL; van Heurn, LWE; De Langen, ZJ; Looyaard, N; Madern, GC; Rieu, PNMA; van der Zee, DC; van Silfhout, M; Aronson, DC
      Quality of life in patients with anorectal malformation or Hirschsprung's disease - Development of a disease-specific questionnaire

      DISEASES OF THE COLON & RECTUM
    69. Potterf, SB; Mollaaghababa, R; Hou, L; Southard-Smith, EM; Hornyak, TJ; Arnheiter, H; Pavan, WJ
      Analysis of SOX10 function in neural crest-derived melanocyte development:SOX10-dependent transcriptional control of dopachrome tautomerase

      DEVELOPMENTAL BIOLOGY
    70. Jacquemin, P; Lannoy, VJ; O'Sullivan, J; Read, A; Lemaigre, FP; Rousseau, GG
      The transcription factor onecut-2 controls the Microphthalmia-associated transcription factor gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    71. Moog, R; Becmeur, F; Kauffmann-Chevalier, I; Sauvage, P
      Hirschsprung's disease and mini-invasive surgery.

      ANNALES DE CHIRURGIE
    72. Santschi, EM; Vrotsos, PD; Purdy, AK; Mickelson, JR
      Incidence of the endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses

      AMERICAN JOURNAL OF VETERINARY RESEARCH
    73. Yamada, K; Yamada, Y; Nomura, N; Miura, K; Wakako, R; Hayakawa, C; Matsumoto, A; Kumagai, T; Yoshimura, I; Miyazaki, S; Kato, K; Sonta, S; Ono, H; Yamanaka, T; Nagaya, M; Wakamatsu, N
      Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features

      AMERICAN JOURNAL OF HUMAN GENETICS
    74. Resendes, BL; Williamson, RE; Morton, CC
      At the speed of sound: Gene discovery in the auditory system

      AMERICAN JOURNAL OF HUMAN GENETICS
    75. Shimotake, T; Go, S; Inoue, K; Tomiyama, H; Iwai, N
      A homozygous missense mutation in the tyrosine kinase domain of the RET proto-oncogene in an infant with total intestinal aganglionosis

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    76. Phay, JE; Moley, JF; Lairmore, TC
      Multiple endocrine neoplasias

      SEMINARS IN SURGICAL ONCOLOGY
    77. Le, HN; Norton, JA
      Perspective on RET proto-oncogene and thyroid cancer

      CANCER JOURNAL
    78. Azuma, T; Seki, N; Yoshikawa, T; Saito, T; Masuho, Y; Muramatsu, M
      cDNA cloning, tissue expression, and chromosome mapping of human homolog of SOX18

      JOURNAL OF HUMAN GENETICS
    79. Dipple, KM; McCabe, ERB
      Modifier genes convert "simple" Mendelian disorders to complex traits

      MOLECULAR GENETICS AND METABOLISM
    80. White, FV; Langer, JC
      Circumferential distribution of ganglion cells in the transition zone of children with Hirschsprung disease

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    81. Hofstra, RMW; Wu, Y; Stulp, RP; Elfferich, P; Osinga, J; Maas, SM; Siderius, L; Brooks, AS; Von der Ende, JJ; Heydendael, VMR; Severijnen, RSVM; Bax, KMA; Meijers, C; Buys, CHCM
      RET and GDNF gene scanning in Hirschprung patients using two dual denaturing gel systems

      HUMAN MUTATION
    82. Rice, J; Doggett, B; Sweetser, DA; Yamagisawa, H; Yanagisawa, M; Kapur, RP
      Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice

      DEVELOPMENTAL DYNAMICS
    83. Ginat, S; Maslen, CL; Conner, WE; Porter, FD; Steiner, RD
      Smith-Lemli-Opitz syndrome: A multiple malformation/mental retardation syndrome caused by defective cholesterol synthesis

      ENDOCRINOLOGIST
    84. Uitto, J; Pulkkinen, L
      The genodermatoses: Candidate diseases for gene therapy

      HUMAN GENE THERAPY
    85. Matera, I; Miguel-Rodriguez, MD; Fernandez-Santos, JM; Santamaria, G; Puliti, A; Ravazzolo, R; Romeo, G; Galera-Davidson, H; Ceccherini, I
      cDNA sequence and genomic structure of the rat RET proto-oncogene

      DNA SEQUENCE
    86. Griseri, P; Sancandi, M; Patrone, G; Bocciardi, R; Hofstra, R; Ravazzolo, R; Devoto, M; Romeo, G; Ceccherini, I
      A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    87. Bondurand, N; Pingault, V; Goerich, DE; Lemort, N; Sock, E; Le Caignec, C; Wegner, M; Goossens, M
      Interaction among SOX10 PAX3 and MITF, three genes altered in Waardenburg syndrome

      HUMAN MOLECULAR GENETICS
    88. Gul, D; Ozturk, H
      Unilateral proximal femoral focal deficiency and Hirschsprung disease

      CLINICAL DYSMORPHOLOGY
    89. Lee, NC; Norton, JA
      Multiple endocrine neoplasia type 2B - genetic basis and clinical expression

      SURGICAL ONCOLOGY-OXFORD
    90. Kelsh, RN; Eisen, JS
      The zebrafish colourless gene regulates development of non-ectomesenchymalneural crest derivatives

      DEVELOPMENT
    91. Schulten, D; Holschneider, AM; Meier-Ruge, W
      Proximal segment histology of resected bowel in Hirschsprung's disease predicts postoperative bowel function

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    92. Becmeur, F; Moog, R; De Luca, G; Christmann, D; Sauvage, P
      Radiological evaluation of Duhamel's operation in Hirschsprung's disease -Attempt at radio-clinical correlation

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    93. Sarioglu, A; Senocak, ME; Hicsonmez, A
      Discordant Hirschsprung's disease in monozygotic twins with concordant congenital deafness

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    94. Valioulis, I; Aubert, D; de Billy, B; Bawab, F; Karam, R
      A complex chromosomal rearrangement associated with Hirschsprung's disease- A case report with a review of the literature

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    95. Moore, SW; Johnson, G; Schneider, JW
      Elevated tissue immunoglobulins in Hirschsprung's disease - Indication of early immunologic response

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    96. Schmittenbecher, PP; Gluck, M; Wiebecke, B; Meier-Ruge, W
      Clinical long-term follow-up results in intestinal neuronal dysplasia (IND)

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    97. Hsu, WM; Wang, W; Chen, CC
      Enteric mucocele formation after endorectal pull-through: Report of a case

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    98. Wegner, M
      Transcriptional control in myelinating glia: The basic recipe

      GLIA
    99. Shin, MK
      Controlling gene expression in mice with tetracycline: Application in pigment cell research

      PIGMENT CELL RESEARCH
    100. Halaban, R
      The regulation of normal melanocyte proliferation

      PIGMENT CELL RESEARCH


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Documento generato il 22/10/20 alle ore 00:31:52