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Neuropediatrics|October 8, 1998
Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutationsA Ohlenbusch, E Wilichowski, F HanefeldLancet (London, England)|September 21, 1996
Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolismS Stöckler, F Hanefeld, J FrahmJournal of Perinatal Medicine|January 1, 1976
The influence of various aminoglycoside preparations on bilirubin/albumin bindingL Ballowitz, F Hanefeld, F SchmidNeuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genesE Wilichowski, A Ohlenbusch, F HanefeldNeuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genesA Ohlenbusch, E Wilichowski, F HanefeldEpilepsia|February 1, 1978
Febrile convulsions and blood-cerebrospinal fluid barrierH Siemes, M Siegert, F HanefeldKlinische Padiatrie|March 1, 1986
[Progressive ataxia and distal muscular atrophy--differential diagnostic considerations on Roussy-Lévy syndrome]F Aksu, H J Christen, F HanefeldRadiology|October 1, 1984
Medullary nephrocalcinosis and pancreatic calcifications demonstrated by ultrasound and CT in infants after treatment with ACTHH P Rausch, F Hanefeld, H J KaufmannMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1987
[Mucolipidosis type II (I-cell disease) with unusually severe heart involvement]R Schulz, J Vogt, W Voss, et al.Neuropadiatrie|August 1, 1976
Protein patterns of the cerebrospinal fluid in children with cerebral palsyH Siemes, M Siegert, D Rating, et al.Pageof 15