Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Shilpa Hundalani"'
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 164
Objective To determine the usefulness of the hour-specific Bhutani et al bilirubin nomogram when applied to infants with Coombs-positive test results. Design Retrospective chart review. Setting Term nursery and neonatal intensive care unit of a unive
Autor:
Girish Hiremath, Aditi Kantipuly, Shilpa Hundalani, Jay R. Shapiro, Sakkubai Naidu, Charles A. Rohde, Theodore Yablonski, Genila Bibat, Michael V. Johnston, Mary E. Blue
Rett Syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene. In 49 female RTT children, ages 1.9–17 years, bone mass was assessed and correlated with clinical parameters and mutations involving the MECP2 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f659335d4b92d455a197ad3d4a636cbf
https://europepmc.org/articles/PMC3074246/
https://europepmc.org/articles/PMC3074246/
Publikováno v:
Annals of Indian Academy of Neurology; Nov2008 Supplement, Vol. 11, pS139-S139, 1/4p