Showing results (11-20 of 86) with videos related to
Sort By:
Pageof 9
Orvosi Hetilap|December 15, 1996
[Alpha thalassemia/metal retardation syndrome--a new X-chromosome linked recessive genetically inherited symptom complex]E Morava, G KosztolányiAmerican Journal of Medical Genetics|July 12, 1996
X-linked mental retardation syndrome: three brothers with the Brooks-Wisniewski-Brown syndromeE Morava, J Storcz, G KosztolányiPediatric Dermatology|February 24, 2001
Complete recovery from juvenile pemphigus vulgarisF Harangi, D Várszegi, I Schneider, et al.Orvosi Hetilap|April 3, 1998
[Extracorporeal membrane oxygenation in neonatology: review of the use of the method]E Morava, W Gill, M PierceClinical Genetics|April 1, 1996
Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndromeE Morava, K Adamovich, A E CzeizelJournal of the European Academy of Dermatology and Venereology : JEADV|July 31, 2007
No significant increase within a 3-year interval in the prevalence of atopic dermatitis among schoolchildren in Baranya County, HungaryF Harangi, A Fogarasy, A Müller, et al.Orvosi Hetilap|February 7, 2002
[Decreased bone mineral density as a risk factor in the development of spinal deformities in neurofibromatosis]V Halmai, K Szász, E Morava, et al.Psychiatrie, Neurologie, Und Medizinische Psychologie|September 1, 1978
[Anticonvulsive treatment and calcium metabolism]A Máttyus, G Bombitz, A Gergely, et al.Clinical Genetics|January 5, 2001
Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian childrenE Morava, M Czakó, B Melegh, et al.Aktuelle Gerontologie|January 1, 1983
Effects of prolonged aminoglutethimid and dehydroepiandrosterone treatment on rat bonesM Boross, E Morava, I Gergely, et al.Pageof 9