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European Journal of Pediatrics|April 1, 1986
Childhood neuromuscular disease with rimmed vacuolesH H Goebel, S von Loh, J Gehler
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1978
Increased urinary excretion of keratan sulfate in fucosidosisH Greiling, H W Stuhlsatz, M Cantz, et al.
AJNR. American Journal of Neuroradiology|May 1, 1983
Cranial computed tomography in disorders of complex carbohydrate metabolism and related storage diseasesB Ludwig, T Kishikawa, S Wende, et al.
Journal of Neurology|January 1, 1984
The value of CT in diagnosis and prognosis of different inborn neurodegenerative disorders in childhoodS Wende, B Ludwig, T Kishikawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristicsJ Gehler, A C Sewell, C Becker, et al.
Helvetica Paediatrica Acta|January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian familyJ Gehler, A C Sewell, C Becker, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|October 23, 1998
[Intravenous immunoglobulins (IVIG) in treatment of an antiphospholipid syndrome in pregnancy]L Heilmann, C Berg, G F von Tempelhoff, et al.
Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1983
Liver pathology in transient neonatal hyperammonemiaA Zimmermann, C Bachmann, I Högger, et al.
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