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Neuropediatrics|June 25, 1998
Marinesco Sjögren syndrome with rhabdomyolysis. A new subtype of the diseaseW Müller-Felber, D Zafiriou, R Scheck, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 5, 2016
[Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series]J Raignoux, U Walther-Louvier, C Espil, et al.
American Journal of Medical Genetics|December 1, 1994
Tetrasomy 21 pter-->q22.1 and Down syndrome: molecular definition of the regionC Daumer-Haas, S Schuffenhauer, J U Walther, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|December 24, 2005
Biphasic chromatin structure and FISH signals in reflect intranuclear orderJyoti P Chaudhuri, Eva Kasprzycki, Mathew Battaglia, et al.
Der Nervenarzt|August 5, 2000
[Gliomatosis cerebri: two case reports with atypical clinical and neuroradiologic findings]P Reich, E U Walther, M Liebetrau, et al.
Neuropediatrics|February 12, 2021
Clinical Phenotype in an Early-Onset French Pediatric Population: Charcot-Marie-Tooth's Disease Type 2AC Majorel-Beraud, E Baudou, U Walther-Louvier, et al.
European Journal of Pediatrics|April 1, 1984
Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndromeH S Heymans, H vd Bosch, R B Schutgens, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
Genomic sequences of aldolase C (Zebrin II) direct lacZ expression exclusively in non-neuronal cells of transgenic miceE U Walther, M Dichgans, S M Maricich, et al.
Lancet (London, England)|July 12, 2005
Acupuncture in patients with osteoarthritis of the knee: a randomised trialC Witt, B Brinkhaus, S Jena, et al.
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