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E V Bawle

Showing results (1-10 of 20) with videos related to

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American Journal of Medical Genetics|January 1, 1994
Osteogenesis imperfecta vs. child abuseE V Bawle
Journal of Inherited Metabolic Disease|January 1, 1991
Chronic coagulopathy in a patient with argininosuccinase deficiencyE V Bawle, I Warrier
American Journal of Diseases of Children (1960)|August 1, 1986
Nonimmune hydrops fetalis in Noonan's syndromeE V Bawle, V Black
The Journal of Dermatology|November 1, 1993
Spontaneous contraction of leukodermic patches in Waardenburg syndromeT Chang, K Hashimoto, E V Bawle
Journal of Inherited Metabolic Disease|July 23, 2003
D-2-Hydroxyglutaric aciduria with absence of corpus callosum and neonatal intracranial haemorrhageX Wang, C Jakobs, E V Bawle
Teratology|May 1, 1998
Adult and two children with fetal methotrexate syndromeE V Bawle, J V Conard, L Weiss
Archives of Pediatrics & Adolescent Medicine|February 15, 2001
Special feature: picture of the month. Bannayan-Ruvalcaba-Riley syndromeR Kaddu, E V Bawle, V Tolia, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 4, 2001
Arginine deficiency-induced hyperammonemia in a home total parenteral nutrition-dependent patient: a case reportS Kapila, M Saba, C H Lin, et al.
Blood|May 15, 1992
Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutationM Maeda, E V Bawle, R Kulkarni, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|December 17, 2008
Blau syndrome (familial granulomatous arthritis, iritis, and rash) in an african-american familyI A Cuesta, E C Moore, R Rabah, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|January 1, 1994
Osteogenesis imperfecta vs. child abuseE V Bawle
Journal of Inherited Metabolic Disease|January 1, 1991
Chronic coagulopathy in a patient with argininosuccinase deficiencyE V Bawle, I Warrier
American Journal of Diseases of Children (1960)|August 1, 1986
Nonimmune hydrops fetalis in Noonan's syndromeE V Bawle, V Black
The Journal of Dermatology|November 1, 1993
Spontaneous contraction of leukodermic patches in Waardenburg syndromeT Chang, K Hashimoto, E V Bawle
Journal of Inherited Metabolic Disease|July 23, 2003
D-2-Hydroxyglutaric aciduria with absence of corpus callosum and neonatal intracranial haemorrhageX Wang, C Jakobs, E V Bawle
Teratology|May 1, 1998
Adult and two children with fetal methotrexate syndromeE V Bawle, J V Conard, L Weiss
Archives of Pediatrics & Adolescent Medicine|February 15, 2001
Special feature: picture of the month. Bannayan-Ruvalcaba-Riley syndromeR Kaddu, E V Bawle, V Tolia, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 4, 2001
Arginine deficiency-induced hyperammonemia in a home total parenteral nutrition-dependent patient: a case reportS Kapila, M Saba, C H Lin, et al.
Blood|May 15, 1992
Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutationM Maeda, E V Bawle, R Kulkarni, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|December 17, 2008
Blau syndrome (familial granulomatous arthritis, iritis, and rash) in an african-american familyI A Cuesta, E C Moore, R Rabah, et al.
Pageof 2