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Pediatric Pathology|January 1, 1986
Glycogen accumulation in the pars recta of the proximal tubule in Fanconi syndromeR W Bendon, G HugAmerican Journal of Obstetrics and Gynecology|August 15, 1985
Morphologic characteristics of the placenta in glycogen storage disease type II (alpha-1,4-glucosidase deficiency)R W Bendon, G HugJournal of Neuro-Oncology|January 1, 1986
Continuous human glioma-derived cell lines UC-11MG and UC-302MG. Morphologic, immunocytochemical and chromosomal characterizationB H Liwnicz, G Archer, S W Soukup, et al.Ultramicroscopy|April 3, 2001
Study of the local atomic strain field in a Zr-doped TiAl intermetallic alloy by EXAFS and ab initio FLAPW calculationsA Ponchel, G Hug, M JaouenAnnals of Surgery|October 1, 1977
Total colectomy and mucosal proctectomy with preservation of continence in ulcerative colitisL W Martin, C LeCoultre, W K SchubertPediatric Research|March 1, 1982
Alpha 1-antitrypsin phenotype: transient cathodal shift in serum of infant girl with urinary cytomegalovirus and fatty liverG Hug, G Chuck, B BowlesJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1980
Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritanceV Ionasescu, G Hug, C HoppelThe Journal of Pediatrics|January 1, 1977
Bile acid malabsorption--a consequence of terminal ileal dysfunction in protracted diarrhea of infancyW F Balistreri, J C Partin, W K SchubertDigestive Diseases and Sciences|February 1, 1983
Hypocalcemia and steatorrhea--clues to etiologyJ E Heubi, J C Partin, W K SchubertThe New England Journal of Medicine|April 19, 1984
Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cellsG Hug, S Soukup, M Ryan, et al.Pageof 8