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    1. Infante, JP; Huszagh, VA
      Impaired arachidonic (20 : 4n-6) and docosahexaenoic (22 : 6n-3) acid synthesis by phenylalanine metabolites as etiological factors in the neuropathology of phenylketonuria

      MOLECULAR GENETICS AND METABOLISM
    2. Douglas, L; Wilson, RD
      Prenatally diagnosed microcephaly: A review of etiologies

      FETAL DIAGNOSIS AND THERAPY
    3. Shield, JPH; Gough, R; Allen, J; Newbury-Ecob, R
      3-hydroxyisobutyric aciduria: phenotypic heterogeneity within a single family

      CLINICAL DYSMORPHOLOGY
    4. Gardner, RJM; Savarirayan, R; Dunne, KB; McLellan, JA; Coleman, LT; Suthers, GK
      Microlissencephaly with cardiac, spinal and urogenital defects

      CLINICAL DYSMORPHOLOGY
    5. Delb, W; Lipfert, S; Henn, W
      Mandibulofacial dysostosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome?

      CLINICAL DYSMORPHOLOGY
    6. de Vries, BBA; van't Hoff, WG; Surtees, RAH; Winter, RM
      Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay

      CLINICAL DYSMORPHOLOGY
    7. Hoffman, HM; Bastian, JF; Bird, LM
      Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome

      CLINICAL DYSMORPHOLOGY
    8. Hadziselimovic, F; Fliegel, C; Miny, P
      A novel syndrome involving primary skeletal growth and retardation in siblings

      CLINICAL DYSMORPHOLOGY
    9. Vivarelli, R; Grosso, S; Cioni, M; Galluzzi, P; Monti, L; Morgese, G; Balestri, P
      Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria

      BRAIN & DEVELOPMENT
    10. Corona-Rivera, JR; Corona-Rivera, E; Rornero-Velarde, E; Hernandez-Rocha, J; Bobadilla-Morales, L; Corona-Rivera, A
      Report and review of the fetal brain disruption sequence

      EUROPEAN JOURNAL OF PEDIATRICS
    11. Hausler, MG; Jaeken, J; Monch, E; Ramaekers, VT
      Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: Report on two siblings

      NEUROPEDIATRICS
    12. Attia-Sobol, J; Encha-Razavi, F; Hermier, M; Vitrey, D; Verloes, A; Plauchu, H
      New syndrome? Lissencephaly type III, stippled epiphyses and loose, thick skin: A new recessively inherited syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    13. Megarbane, A; Waked, N; Chouery, E; Moglabey, YB; Saliba, N; Mornet, E; Serre, JL; Slim, R
      Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    14. Kondoh, T; Yamamoto, T; Kono, Y; Matsumoto, T; Sugawara, H; Matsumoto, N; Moriuchi, H
      Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: A new autosomalrecessive MCA/MR syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Verloes, A; Dresse, MF; Keutgen, H; Asplund, C; Smith, CIE
      Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Silengo, M; Del Monaco, A; Linari, A; Lala, R
      Low birth-weight, microcephalic malformation syndrome in a 46,XX girl and her 46,XY sister with agonadism: Third report of the Kennerknecht syndrome or autosomal recessive Seckel-like syndrome with previously undescribed genital anomalies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Megarbane, A; Delague, V; Ruchoux, MM; Rizkallah, E; Maurage, CA; Viollet, L; Rouaix-Emery, N; Urtizberea, A
      New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Ross, ME; Walsh, CA
      Human brain malformations and their lessons for neuronal migration

      ANNUAL REVIEW OF NEUROSCIENCE
    19. Schmeling, H; Wohlrab, J; Mathony, K; Gaber, G; Lieser, U; Burdach, S; Horneff, G
      Incontinentia pigmenti Bloch-Sulzberger. Case report

      MONATSSCHRIFT KINDERHEILKUNDE
    20. Villo, N; Beceiro, J; Cebrero, M; de Frias, EG
      Fetal brain disruption sequence in a newborn infant with a history of cordocentesis at 21 weeks gestation

      ARCHIVES OF DISEASE IN CHILDHOOD
    21. Fabian, VA; Nelson, J; Smith, NM; Urich, H
      Lethal X-linked microcephaly with dysmorphic features, bilateral optic pathway aplasia and normal eyes

      ACTA NEUROPATHOLOGICA
    22. Koch, R; Hanley, W; Levy, H; Matalon, R; Rouse, B; Trefz, F; Guttler, F; Azen, C; Friedman, E; Platt, L; de la Cruz, F
      Maternal phenylketonuria: An international study

      MOLECULAR GENETICS AND METABOLISM
    23. Caviness, VS; Takahashi, T; Nowakowski, RS
      Neocortical malformation as consequence of nonadaptive regulation of neuronogenetic sequence

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    24. Wang, D; Kranz-Eble, P; De Vivo, DC
      Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome

      HUMAN MUTATION
    25. Abdel-Salam, G; Czeizel, AE
      A case-control etiologic study of microcephaly

      EPIDEMIOLOGY
    26. Abdel-Salam, GMH; Svekus, A; Pelle, Z; Halasz, AA; Czeizel, AE
      Microcephaly, microphthalmia, congenital cataract, with calcification of the basal ganglia: MCA/MR syndrome

      GENETIC COUNSELING
    27. Rajab, A; Riaz, A; Paul, G; Al-Khusaibi, S; Chalmers, R; Patton, MA
      Further delineation of the DOOR syndrome

      CLINICAL DYSMORPHOLOGY
    28. Abdel-Salam, G; Czeizel, AE
      The second unrelated case with isolated microcephaly and normal intelligence (Microcephalia vera)

      CLINICAL DYSMORPHOLOGY
    29. Plomp, AS; Baraitser, M; Slaney, SF; Winter, RM
      Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?

      CLINICAL DYSMORPHOLOGY
    30. Petek, E; Kostl, G; Mutz, I; Wagner, K; Kroisel, PM
      Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH

      CLINICAL DYSMORPHOLOGY
    31. Lam, YH; Tang, MHY
      Serial sonographic features of a fetus with hydranencephaly from 11 weeks to term

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    32. Den Hollander, NS; Wessels, MW; Los, FJ; Ursem, NTC; Niermeijer, MF; Wladimiroff, JW
      Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significance

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    33. Inouye, M; Takahashi, S; Kubota, Y; Hayasaka, S; Murata, Y
      Similarity between the effects of carbon-ion irradiation and X-irradiationon the development of rat brain

      JOURNAL OF RADIATION RESEARCH
    34. Nassogne, MC; Henrot, B; Aubert, G; Bonnier, C; Marie, S; Saint-Martin, C; Van den Berghe, G; Sebire, G; Vincent, MF
      Adenylosuccinase deficiency: an unusual cause of early-onset epilepsy associated with acquired microcephaly

      BRAIN & DEVELOPMENT
    35. Coppola, G; Muras, I; Pascotto, A
      Pontocerebellar hypoplasia type 2 (PCH2): report of two siblings

      BRAIN & DEVELOPMENT
    36. Custer, DA; Vezina, LG; Vaught, DR; Brasseux, C; Samango-Sprouse, CA; Cohen, MS; Rosenbaum, KN
      Neurodevelopmental and neuroimaging correlates in nonsyndromal microcephalic children

      JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
    37. Simonati, A; Santorum, E; Tessa, A; Polo, A; Simonetti, F; Bernardina, BD; Santorelli, FM; Rizzuto, N
      A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL

      NEUROPEDIATRICS
    38. Nassogne, MC; Henrot, B; Saint-Martin, C; Kadhim, H; Dobyns, WB; Sebire, G
      Polymicrogyria and motor neuropathy in micro syndrome

      NEUROPEDIATRICS
    39. Pavone, P; Parano, E; Polizzi, A; Trifiletti, RR
      Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    40. Buttiker, V; Wojtulewicz, J; Wilson, M
      Imperforate anus in Feingold syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Niesen, CE; Shah, NS
      Pyridostigmine-induced microcephaly

      NEUROLOGY
    42. Kleier, S; Herrmann, M; Wittwer, B; Varon, R; Reis, A; Horst, J
      Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome

      CLINICAL GENETICS
    43. Ono-Yagi, K; Ohno, M; Iwami, M; Takano, T; Yamano, T; Shimada, M
      Heterotopia in microcephaly induced by cytosine arabinoside: hippocampus in the neocortex

      ACTA NEUROPATHOLOGICA
    44. Kawame, H; Sugio, Y; Fuyama, Y; Hagashi, Y; Suzuki, H; Kurosawa, K; Maekawa, K
      Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD):report of a new case and review of the literature

      JOURNAL OF HUMAN GENETICS
    45. Arnold, SR; Spicer, D; Kouseff, B; Lacson, A; Gilbert-Barness, E
      Seckel-like syndrome in three siblings

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    46. Roberts, E; Jackson, AP; Carradice, AC; Deeble, VJ; Mannan, J; Rashid, Y; Jafri, H; McHale, DP; Markham, AF; Lench, NJ; Woods, CG
      The second locus for autosomal recessive primary microcephaly (MCPH2) mapsto chromosome 19q13.1-13.2

      EUROPEAN JOURNAL OF HUMAN GENETICS
    47. Criado, GR; Rufo, M; de Terreros, IG
      A second family with Micro syndrome

      CLINICAL DYSMORPHOLOGY
    48. Kreuz, FR; Nolte-Buchholtz, S; Fackler, F; Behrens, R
      Another case of achalasia-microcephaly syndrome

      CLINICAL DYSMORPHOLOGY
    49. Cassidy, L; Taylor, D
      Congenital cataract and multisystem disorders

      EYE
    50. Kivitie-Kallio, S; Larsen, A; Kajasto, K; Norio, R
      Neurological and psychological findings in patients with Cohen syndrome: Astudy of 18 patients aged 11 months to 57 years

      NEUROPEDIATRICS
    51. Fombonne, E; Roge, B; Claverie, J; Courty, S; Fremolle, J
      Microcephaly and macrocephaly in autism

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    52. Williams, MS; Williams, JL; Wargowski, DS; Pauli, RM; Pletcher, BA
      Filippi syndrome: Report of three additional cases

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. Guion-Almeida, ML; Zechi-Ceide, RM; Richieri-Costa, A
      Multiple congenital anomalies syndrome: Growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Achermann, S; Largo, R; Kotzot, D; Riegel, M; Schinzel, A
      Short stature, myopia, severe developmental delay, and peculiar facial appearance in two brothers: A new syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. Criado, GR; Aytes, AP
      Mobius sequence, hypogenitalism, cerebral, and skeletal malformations in two brothers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Limwongse, C; Wyszynski, RE; Dickerman, LH; Robin, NH
      Microcephaly-lymphedema-chorioretinal dysplasia: A unique genetic syndromewith variable expression and possible characteristic facial appearance

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Pagnan, NAB; Ribeiro, EMDF; Poerner, F
      Say syndrome: Report of a familial case

      AMERICAN JOURNAL OF MEDICAL GENETICS
    58. Slee, J; Lam, G; Walpole, I
      Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification

      AMERICAN JOURNAL OF MEDICAL GENETICS
    59. Shrimpton, AE; Daly, KM; Hoo, JJ
      Mapping of a gene (MRXS9) for X-linked mental Retardation, microcephaly, and variably short stature to Xq12-q21.31

      AMERICAN JOURNAL OF MEDICAL GENETICS
    60. Peiffer, A; Singh, N; Leppert, M; Dobyns, WB; Carey, JC
      Microcephaly with simplified gyral pattern in six related children

      AMERICAN JOURNAL OF MEDICAL GENETICS
    61. Elliott, AM; Graham, GE; Bernstein, M; Mazer, B; Teebi, AS
      Dyskeratosis congenita: An autosomal recessive variant

      AMERICAN JOURNAL OF MEDICAL GENETICS
    62. Megarbane, A; Haddad-Zebouni, S; Nabbout, R; Khoury, AH; Traboulsi, EI
      Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: A new MCA/MR syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    63. Meyers, KEC; Kaplan, P; Kaplan, BS
      Nephrotic syndrome, microcephaly, and developmental delay: Three separate syndromes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    64. Azuri, J; Mizrachi, A; Weintraub, S; Lerman-Sagie, T
      Neurological involvement in a child with the wrinkly skin syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    65. Janssen, HCJP; Schaap, C; Vandevijver, N; Moerman, P; de Die-Smulders, CEM; Fryns, JP
      Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

      JOURNAL OF MEDICAL GENETICS
    66. Brooks, AS; Breuning, MH; Osinga, J; Van der Smagt, JJ; Catsman, CE; Buys, CHCM; Meijers, C; Hofstra, RMW
      A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)

      JOURNAL OF MEDICAL GENETICS
    67. Kennedy, SJ; Lee, KJ; McCrindle, BW; Teebi, AS
      Microcephaly-cardiomyopathy syndrome: confirmation of the phenotype

      JOURNAL OF MEDICAL GENETICS
    68. Sarkisian, MR; Rattan, S; D'Mello, SR; LoTurco, JJ
      Characterization of seizures in the flathead rat: A new genetic model of epilepsy in early postnatal development

      EPILEPSIA
    69. Bartolomei, F; Gavaret, M; Dravet, C; Guerrini, R
      Familial epilepsy with unilateral and bilateral malformations of cortical development

      EPILEPSIA
    70. Weber, KM; Kousseff, BG
      'New' manifestations of BOR syndrome

      CLINICAL GENETICS
    71. Hanley, WB; Platt, LD; Bachman, RP; Buist, N; Geraghty, MT; Isaacs, J; O'Flynn, ME; Rhead, WJ; Seidlitz, G; Tishler, B
      Undiagnosed maternal phenylketonuria: The need for prenatal selective screening or case finding

      AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
    72. ten Donkelaar, HJ; Wesseling, P; Semmekrot, BA; Liem, KD; Tuerlings, J; Cruysberg, JRM; de Wit, PEJ
      Severe, non X-linked congenital microcephaly with absence of the pyramidaltracts in two siblings

      ACTA NEUROPATHOLOGICA
    73. Tsukahara, M; Sugio, Y
      New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation

      JOURNAL OF HUMAN GENETICS
    74. ATCHANEEYASAKUL LO; LINCK L; WELEBER RG
      MICROCEPHALY WITH CHORIORETINAL DEGENERATION

      Ophthalmic genetics
    75. STEINMULLER R; STEINBERGER D; MULLER U
      MEHMO (MENTAL-RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND GENITALISM, MICROCEPHALY, OBESITY), A NOVEL SYNDROME - ASSIGNMENT OF DISEASE LOCUS TO XP21.1-P22.13

      European journal of human genetics
    76. Greene, CS
      Pancraniosynostosis after surgery for single sutural craniosynostosis

      PEDIATRIC NEUROSURGERY
    77. ALDABBOUS R; SABRY MA; FARAH S; ALAWADI SA; SIMEONOV S; FARAG TI
      THE AUTOSOMAL RECESSIVE CONGENITAL INTRAUTERINE INFECTION-LIKE SYNDROME OF MICROCEPHALY, INTRACRANIAL CALCIFICATION, AND CNS DISEASE - REPORT OF ANOTHER BEDOUIN FAMILY

      Clinical dysmorphology
    78. PILU G; FALCO P; MILANO V; PEROLO A; BOVICELLI L
      PRENATAL-DIAGNOSIS OF MICROCEPHALY ASSISTED BY VAGINAL SONOGRAPHY ANDPOWER DOPPLER

      Ultrasound in obstetrics & gynecology
    79. MAUCERI L; BAIELI S; RIZZO R; BIANCA S; MATTINA T
      TRIPLE-X CONSTITUTION IN A CHILD WITH MULTIPLE CONGENITAL-ANOMALIES

      Rivista italiana di pediatria
    80. HASHIMOTO K; TAKEUCHI Y; KIDA Y; HASEGAWA H; KANTAKE M; SASAKI A; ASANUMA K; ISUMI H; TAKASHIMA S
      3 SIBLINGS OF FATAL INFANTILE ENCEPHALOPATHY WITH OLIVOPONTOCEREBELLAR HYPOPLASIA AND MICROCEPHALY

      Brain & development
    81. IPPEL PF; BRESLAUSIDERIUS EJ; HACK WWM; VANDERBLIJ HF; BOUVE S; BIJLSMA JB
      ATELENCEPHALIC MICROCEPHALY - A CASE-REPORT AND REVIEW OF THE LITERATURE

      European journal of pediatrics
    82. COGSWELL CA; SARKISIAN MR; LEUNG V; PATEL R; DMELLO SR; LOTURCO JJ
      A GENE ESSENTIAL TO BRAIN GROWTH AND DEVELOPMENT MAPS TO THE DISTAL ARM OF RAT-CHROMOSOME-12

      Neuroscience letters
    83. BARKOVICH AJ; FERRIERO DM; BARR RM; GRESSENS P; DOBYNS WB; TRUWIT CL; EVRARD P
      MICROLISSENCEPHALY - A HETEROGENEOUS MALFORMATION OF CORTICAL DEVELOPMENT

      Neuropediatrics
    84. STRAUSSBERG R; KORNREICH L; HAREL L; VARSANO I
      AUTOSOMAL RECESSIVE MICROCEPHALY WITH NEONATAL MYOCLONIC SEIZURES - CLINICAL AND MRI FINDINGS

      American journal of medical genetics
    85. HARRISON KJ; TESHIMA IE; SILVER MM; JAY V; UNGER S; ROBINSON WP; JAMES A; LEVIN A; CHITAYAT D
      PARTIAL TETRASOMY WITH TRIPLICATION OF CHROMOSOME (5) (P14-P15.33) INA PATIENT WITH SEVERE MULTIPLE CONGENITAL-ANOMALIES

      American journal of medical genetics
    86. RAYNAUD M; RONCE N; AYRAULT AD; FRANCANNET C; MALPUECH G; MORAINE C
      X-LINKED MENTAL-RETARDATION WITH ISOLATED GROWTH-HORMONE DEFICIENCY IS MAPPED TO XQ22-XQ27.2 IN ONE FAMILY

      American journal of medical genetics
    87. KUMAR D; RITTEY C; CAMERON AH; VARIEND S
      RECOGNIZABLE INHERITED SYNDROME OF PROGRESSIVE CENTRAL-NERVOUS-SYSTEMDEGENERATION AND GENERALIZED INTRACRANIAL CALCIFICATION WITH OVERLAPPING PHENOTYPE OF THE SYNDROME OF AICARDI AND GOUTIERES

      American journal of medical genetics
    88. Groen, SE; Drewes, JG; de Boer, EG; Hoovers, JMN; Hennekam, RCM
      Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6

      AMERICAN JOURNAL OF MEDICAL GENETICS
    89. Strenge, S; Froster, UG
      Microcephaly-lymphedema syndrome: Report of a family with short stature asadditional manifestation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    90. Duval, A; Boute, O; Devisme, L; Valat, AS; Manouvrier, S
      New autosomal recessive syndrome of severe microcephaly and skeletal anomalies including posterior rib-gap defects

      AMERICAN JOURNAL OF MEDICAL GENETICS
    91. TEEBI AS; MILLER S; OSTRER H; EYDOUX P; COLOMBBROCKMANN C; OUDJHANE K; WATTERS G
      SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY WITH NORMAL INTELLIGENCE, AND XY SEX REVERSAL - A NEW AUTOSOMAL RECESSIVE SYNDROME

      Journal of Medical Genetics
    92. MOWAT DR; CROAKER GDH; CASS DT; KERR BA; CHAITOW J; ADIS LC; CHIA NL; WILSON MJ
      HIRSCHSPRUNG-DISEASE, MICROCEPHALY, MENTAL-RETARDATION, AND CHARACTERISTIC FACIAL FEATURES - DELINEATION OF A NEW SYNDROME AND IDENTIFICATION OF A LOCUS AT CHROMOSOME 2Q22-Q23

      Journal of Medical Genetics
    93. CHEVASSUSAULOUIS N; RAFIKI A; JORQUERA I; BENARI Y; REPRESA A
      NEOCORTEX IN THE HIPPOCAMPUS - AN ANATOMICAL AND FUNCTIONAL-STUDY OF CA1 HETEROTOPIAS AFTER PRENATAL TREATMENT WITH METHYLAZOXYMETHANOL IN RATS

      Journal of comparative neurology
    94. CHEVASSUSAULOUIS N; BENARI Y; VERGNES M
      DECREASED SEIZURE THRESHOLD AND MORE RAPID RATE OF KINDLING IN RATS WITH CORTICAL MALFORMATION INDUCED BY PRENATAL TREATMENT WITH METHYLAZOXYMETHANOL

      Brain research
    95. RAFIKI A; CHEVASSUSAULOUIS N; BENARI Y; KHRESTCHATISKY M; REPRESA A
      GLUTAMATE RECEPTORS IN DYSPLASIC CORTEX - AN IN-SITU HYBRIDIZATION AND IMMUNOHISTOCHEMISTRY STUDY IN RATS WITH PRENATAL TREATMENT WITH METHYLAZOXYMETHANOL

      Brain research
    96. FUNAHASHI A; FUJIMIYA M; KIMURA H; MAEDA T
      ABNORMAL-DEVELOPMENT OF SEROTONIN NERVE-FIBERS IN THE VISUAL-CORTEX IN RATS WITH METHYLAZOXYMETHANOL-INDUCED MICROCEPHALY

      Acta Neuropathologica
    97. VANGENDEREN MM; SCHUIL J; MEIRE FM
      MICROCEPHALY WITH CHORIORETINOPATHY - A REPORT OF 2 DOMINANT FAMILIESAND 3 SPORADIC CASES

      Ophthalmic genetics
    98. NAIDU S
      RETT-SYNDROME - NATURAL-HISTORY AND UNDERLYING DISEASE MECHANISMS

      European child & adolescent psychiatry
    99. HORN D; MULLER D; THIELE H; KUNZE J
      EXTREME MICROCEPHALY, SEVERE GROWTH AND MENTAL-RETARDATION, FLEXION CONTRACTURES, AND ICHTHYOTIC SKIN IN 2 BROTHERS - A NEW SYNDROME OR MILD FORM OF NEU-LAXOVA-SYNDROME

      Clinical dysmorphology
    100. MILUNSKY JM; GENEST DR; MILUNSKY A
      RENAL TUBULAR DYSGENESIS WITH MICROCEPHALY

      Pediatric nephrology


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Documento generato il 22/10/20 alle ore 15:17:38