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Archives of Disease in Childhood|July 20, 2007
Outcome in children with brain tumours diagnosed in the first year of life: long-term complications and quality of lifeN U Gerber, D Zehnder, T J Zuzak, et al.American Journal of Medical Genetics|July 23, 1998
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping"A Superti-Furga, R Tenconi, M Clementi, et al.European Journal of Pediatrics|May 1, 1994
A syndrome of primary combined immunodeficiency with microcephaly, cerebellar hypoplasia, growth failure and progressive pancytopeniaF Berthet, R Caduff, U B Schaad, et al.Human Genetics|October 28, 1997
Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCRS Kleinle, U Wiesmann, A Superti-Furga, et al.Journal of Computer Assisted Tomography|September 1, 1990
MR imaging of brain maturation in normal and developmentally handicapped childrenE Martin, C Boesch, M Zuerrer, et al.Helvetica Paediatrica Acta|August 1, 1988
[Magnetic resonance in pediatric research and clinical practice. II. Studies on the development and pathology of the brain in neonates, infants and young children]E Martin, C Boesch, R Grütter, et al.Neuropediatrics|December 1, 1994
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1C Kuenzle, M Weissert, E Roulet, et al.Eye (London, England)|May 23, 2009
Ophthalmological findings in Joubert syndromeV Sturm, H Leiba, M N Menke, et al.Neuropediatrics|July 30, 2009
Pontine tegmental cap dysplasia: the severe end of the clinical spectrumC Rauscher, A Poretti, T M Neuhann, et al.Neuromuscular Disorders : NMD|January 1, 1991
X-linked centronuclear myopathy: mapping the gene to Xq28S Liechti-Gallati, B Müller, T Grimm, et al.Pageof 759