Showing results (1731-1740 of 4,819) with videos related to
Sort By:
Pageof 482
Brain & Development|May 9, 2020
Mitochondrial carbonic anhydrase VA deficiency in three Indian infants manifesting early metabolic crisisRamesh Konanki, Radha Rama Devi Akella, Nalinikanta Panigrahy, et al.Brain & Development|January 1, 1989
Incidence and causes of intracranial hemorrhage in infancy: a prospective surveillance study after vitamin K prophylaxisT Matsuzaka, M Yoshinaga, Y Tsuji, et al.Brain & Development|January 1, 1989
Ocular findings in Fukuyama type congenital muscular dystrophyA Tsutsumi, Y Uchida, M Osawa, et al.Brain & Development|January 1, 1989
Secondary amenorrhea in two sisters with hypogonadotropic hypogonadism and progressive cerebellar ataxiaA Arlazoroff, T Rosenberg, N Gadoth, et al.Brain & Development|July 2, 2015
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorderSanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, et al.Brain & Development|May 23, 2015
Phenytoin toxicity in two-month-old Thai infant with CYP2C9 gene polymorphism--A case reportMontida Veeravigrom, Vorapol Jaroonvanichkul, Wiracha Netbaramee, et al.Brain & Development|June 2, 2015
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduriaYupeng Liu, Xiyuan Li, Qiao Wang, et al.Brain & Development|June 22, 2015
Late-onset epileptic spasms in a patient with 22q13.3 deletion syndromeNobutsune Ishikawa, Yoshiyuki Kobayashi, Yuji Fujii, et al.Brain & Development|January 1, 1982
Mortality and clinical features in cases of death among epileptic childrenT Kurokawa, K C Fung, T Hanai, et al.Brain & Development|January 1, 1982
Facial hemangioma with cerebrovascular anomalies and cerebellar hypoplasiaY Mizuno, T Kurokawa, Y Numaguchi, et al.Pageof 482