Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Kabra

Showing results (71-80 of 121) with videos related to

Pageof 13
Sort By:
Indian Pediatrics|October 1, 1995
Clinical and biochemical studies in homocystinuriaM Kaur, M Kabra, G P Das, et al.
Indian Journal of Pediatrics|May 8, 2001
Hypocalcemic heart failure masquerading as dilated cardiomyopathyS Gulati, A Bajpai, R Juneja, et al.
Clinical Chemistry|February 1, 1980
Simultaneous liquid-chromatographic determination of zinc protoporphyrin IX, protoporphyrin IX, and coproporphyrin in whole bloodG R Gotelli, J H Wall, P M Kabra, et al.
Indian Journal of Pediatrics|June 16, 2001
Congenital myotonic dystrophyS Gulati, M Kabra, S Gera, et al.
Indian Journal of Pediatrics|December 6, 2000
Infantile-onset leukoencephalopathy with discrepant mild clinical courseS Gulati, M Kabra, S Gera, et al.
Indian Pediatrics|June 27, 2000
Idiopathic cranio-osteoarthropathyM Kabra, S K Kabra, M Ghosh, et al.
Indian Pediatrics|March 1, 1992
Significance of cord problems at birthS Kumari, A Saxena, D Monga, et al.
European Journal of Clinical Nutrition|April 24, 2014
Prevalence of neonatal hypothyroidism in Kangra Valley, Himachal PradeshU Kapil, V Jain, M Kabra, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 28, 2001
Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyR Mathur, P S Menon, M Kabra, et al.
Indian Pediatrics|November 1, 1996
Menkes' Kinky Hair disease: new considerationsM Kabra, A K Gangakhedkar, G R Pasi, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Indian Pediatrics|October 1, 1995
Clinical and biochemical studies in homocystinuriaM Kaur, M Kabra, G P Das, et al.
Indian Journal of Pediatrics|May 8, 2001
Hypocalcemic heart failure masquerading as dilated cardiomyopathyS Gulati, A Bajpai, R Juneja, et al.
Clinical Chemistry|February 1, 1980
Simultaneous liquid-chromatographic determination of zinc protoporphyrin IX, protoporphyrin IX, and coproporphyrin in whole bloodG R Gotelli, J H Wall, P M Kabra, et al.
Indian Journal of Pediatrics|June 16, 2001
Congenital myotonic dystrophyS Gulati, M Kabra, S Gera, et al.
Indian Journal of Pediatrics|December 6, 2000
Infantile-onset leukoencephalopathy with discrepant mild clinical courseS Gulati, M Kabra, S Gera, et al.
Indian Pediatrics|June 27, 2000
Idiopathic cranio-osteoarthropathyM Kabra, S K Kabra, M Ghosh, et al.
Indian Pediatrics|March 1, 1992
Significance of cord problems at birthS Kumari, A Saxena, D Monga, et al.
European Journal of Clinical Nutrition|April 24, 2014
Prevalence of neonatal hypothyroidism in Kangra Valley, Himachal PradeshU Kapil, V Jain, M Kabra, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 28, 2001
Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyR Mathur, P S Menon, M Kabra, et al.
Indian Pediatrics|November 1, 1996
Menkes' Kinky Hair disease: new considerationsM Kabra, A K Gangakhedkar, G R Pasi, et al.
Pageof 13