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Nanisme microcéphalique, arriération sévère, hypertonie, obésité et hypog&nitalisme chez deux frères : un nouveau syndrome? = Two brothers with severe mental and growth retardation, microcephaly, hypertonicity, obesity and hypogenitalism: a new syndromeDELOZIER-BLANCHET, C. D; HAENGGELI, C. A; ENGEL, E et al.Journal de génétique humaine. 1989, Vol 37, Num 4-5, pp 353-365, issn 0021-7743, 13 p.Article

A prospective study of the accuracy of ultrasound in predicting fetal microcephalyCHERVENAK, F. A; ROSENBERG, J; BRIGHTMAN, R. C et al.Obstetrics and gynecology (New York. 1953). 1987, Vol 69, Num 6, pp 908-910, issn 0029-7844Article

Atelencephalic microcephaly: craniofacial anatomy and morphologic comparisons with holoprosencephaly and anencephalySIEBERT, J. R; KOKICH, V. G; WARKANY, J et al.Teratology (Philadelphia, PA). 1987, Vol 36, Num 3, pp 279-285, issn 0040-3709Article

Microcephaly with short stature, macrocytosis, and pancytopeniaDEBAUN, M. R; WALL, D. A; WATSON, M. S et al.The American journal of pediatric hematology/oncology. 1993, Vol 15, Num 3, pp 356-360, issn 0192-8562Article

Disproportionate intra-uterine head growth and developmental outcomeBRENNAN, T. L; FUNK, S. G; FROTHINGHAM, T. E et al.Developmental medicine and child neurology (Print). 1985, Vol 27, Num 6, pp 746-750, issn 0012-1622Article

Nanisme microcéphalique primordial de type II : à propos d'un cas ayant terminé sa croissance = Type II primordial microcephalic dwarfism. Report of a patient with completed growthTHEAU, D; MAROTEAUX, P.Annales de pédiatrie (Paris). 1993, Vol 40, Num 5, pp 323-328, issn 0066-2097Article

Microcéphalie familiale héréditaire: étude clinique et génétique à propos de cinq cas = Familial hereditary microcephaly. Clinical and genetic findings in five casesNORES, J. M; VINOGRADOFF, M; BAROIS, A et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 26, pp 1619-1622, issn 0037-1777Article

Growth hormone treatment in children with sporadic primary microcephalySPADONI, G. L; CIANFARANI, S; BERNARDINI, S et al.American journal of diseases of children (1960). 1989, Vol 143, Num 11, pp 1282-1283, issn 0002-922X, 2 p.Article

Autosomal recessive nonsyndromal microcephaly with normal intelligenceTEEBI, A. S; AL-AWADI, S. A; WHITE, A. G et al.American journal of medical genetics. 1987, Vol 26, Num 2, pp 355-359, issn 0148-7299Article

Microcephaly: a review of genetic implications in its causationCOWIE, V. A.Journal of mental deficiency research. 1987, Vol 31, Num 3, pp 229-233, issn 0022-264XArticle

Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationHORI, A; TAMAGAWA, K; EBER, S. W et al.Acta neuropathologica. 1987, Vol 74, Num 4, pp 397-401, issn 0001-6322Article

Reduction of disruptive mealtime behavior by facial screening. A case study of a mentally retarded girl with long-term follow-upHORTON, S. V.Behavior modification. 1987, Vol 11, Num 1, pp 53-64, issn 0145-4455Article

GMS syndrome : a new dominant condition with goniodysgenesis, mental retardation, and short statureKUPCHIK, G. S; LUDMAN, M. D; RAAB, E. L et al.American journal of medical genetics. 1992, Vol 42, Num 1, pp 1-4, issn 0148-7299Article

Microencephaly: cortical hypoplasia induced by methylazoxymethanolSANBERG, P. R; MORAN, T. H; COYLE, J. T et al.Neurology and neurobiology. 1987, Vol 33, pp 253-278, issn 0736-4563Article

Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed earsHURST, J. A; WINTER, R. M; BARAITSER, M et al.American journal of medical genetics. 1988, Vol 29, Num 1, pp 107-115, issn 0148-7299Article

Neu laxova syndrome in two Egyptian familiesABDEL MEGUID, N; TEMTAMY, S. A.American journal of medical genetics. 1991, Vol 41, Num 1, pp 30-31, issn 0148-7299Article

Nager anomaly with severe facial involvement, microcephaly, and mental retardationPALOMEQUE, A; PASTOR, X; BALLESTA, F et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 356-357, issn 0148-7299, 2 p.Article

Syndrome familial associant : nanisme, microcéphalie, oligophrénie, épilepsie, surdité de dermatose. Un nouveau syndrome = Familial syndrome combining short stature, microcephaly, mental deficiency, seizures, hearing loss, and skin lesions: a new syndromeBOUDHINA, T; YEDES, A; KHIARI, S et al.Annales de pédiatrie (Paris). 1990, Vol 37, Num 6, pp 399-403, issn 0066-2097Article

Two brothers with facial anomalies, microcephaly, hypoplastic genitalia, and a failure of psychomotor developmentMACDERMOT, K. D; WINTER, R. M.American journal of medical genetics. 1989, Vol 32, Num 1, pp 60-62, issn 0148-7299, 3 p.Article

Microcephaly and intelligenceMEADOW, R.Developmental medicine and child neurology (Print). 1991, Vol 33, Num 3, pp 267-272, issn 0012-1622Article

Increased uptake sites for serotonin and dopamine with decreased S2 serotonin receptors in microencephalic rat brainWATANABE, M; KINUYA, M; MAMIYA, G et al.Neurochemical research. 1990, Vol 15, Num 10, pp 1017-1022, issn 0364-3190, 6 p.Article

The dilemma in prenatal diagnosis of idiopathic microcephalyJAFFE, M; TIROSH, E; OREN, S et al.Developmental medicine and child neurology (Print). 1987, Vol 29, Num 2, pp 187-189, issn 0012-1622Article

Computed tomography of the head in the evaluation of microcephalyJAWORSKI, M; HERSH, J. H; DONAT, J et al.Pediatrics (Evanston). 1986, Vol 78, Num 6, pp 1064-1069, issn 0031-4005Article

Early prenatal diagnosis of genetic microcephalyNGUYEN THE, H; PESCIA, G; DEONNA, T et al.Prenatal diagnosis. 1985, Vol 5, Num 5, pp 345-347, issn 0197-3851Article

Case 27-2014: A 10-Month-Old Boy with Microcephaly and Episodic CyanosisSAHAI, Inderneel; MOCHIDA, Ganeshwaran H; GRABOWSKI, Eric F et al.The New England journal of medicine. 2014, Vol 371, Num 9, pp 847-858, issn 0028-4793, 12 p.Article

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