Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Naznin Dixit"'
Autor:
Josephine Stout, Naznin Dixit, Simeen Pasha, Anju Sukumaran, Ali Kemal Topaloglu, Mary K. Armstrong, Padma Garg, Cynthia Karlson, John T. Bates, Md Abu Yusuf Ansari, Fariha Kamran
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 4, Pp 234-241 (2024)
Purpose The coronavirus disease 2019 (COVID-19) pandemic has led to an association between COVID-19 and pediatric diabetes. Studies have indicated the increased likelihood of children with COVID-19 infection developing diabetes. Our objective was to
Externí odkaz:
https://doaj.org/article/3e20d54516a341fd99daa16643935420
Publikováno v:
Pharmaceuticals, Vol 3, Iss 4, Pp 1279-1285 (2010)
In the United States non-steroidal anti-inflammatory drugs (NSAID) are freely available over-the-counter. Because of the adverse effects on the kidneys and the popularity of these drugs, unregulated use of NSAIDs is an under recognized and potentiall
Externí odkaz:
https://doaj.org/article/6bddb656e1154c2789a5f1b6d9069780
Autor:
NAZNIN DIXIT, SIMEEN PASHA, ANJU P. SUKUMARAN, KATELYN ARMSTRONG, KEMAL TOPALOGLU, LAUREN GHOLSON, FARIHA KAMRAN
Publikováno v:
Diabetes. 71
Background: Mississippi ranks second for childhood obesity prevalence (22%) above the national average of 16 % with significant racial and health disparities. Since March 2020, stay-at home orders, virtual learning, stress, and poor lifestyle may hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7fdba83a1b24f431b00fc9ccd2b520c
https://doi.org/10.2337/db22-982-p
https://doi.org/10.2337/db22-982-p
Publikováno v:
Journal of the Endocrine Society
Background: Neonatal thyrotoxicosis is rare but can be life threatening. This usually has an autoimmune etiology occurring due to transplacental passage of TSH receptor-stimulating immunoglobulins (TSI) from mother to fetus. Perinatal monitoring for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a68734f37d222dca246eefa9ad56845d
http://europepmc.org/articles/PMC6553400
http://europepmc.org/articles/PMC6553400
Publikováno v:
Nephrology. 9:381-386
SUMMARY: Background: Henoch–Schonlein purpura (HSP) is a vasculitic syndrome with palpable purpura and renal involvement. The treatment for HSP with persistent renal disease remains controversial. The kidney biopsy in HSP shows IgA deposits and fis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::377ff725dd439c4960d44b4ecc656c22
https://doi.org/10.1111/j.1440-1797.2004.00320.x
https://doi.org/10.1111/j.1440-1797.2004.00320.x
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Biomembranes. 1667(2):114-121
The kidney plays a major role in reabsorption of phosphate with the majority occurring in the proximal tubule (PT). The type IIa sodium-phosphate co-transporter (NaPi-IIa) is the main player in PT. The purpose of current study was to determine the ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::603e975b64de030fc3d6dd425932fb99
Autor:
Michael J. Schumacher, Naznin Dixit, Mehul Dixit, John J. Hutter, Raymond B. Nagle, Katherine M. Scott, Erika Bracamonte
Publikováno v:
Pediatric Nephrology. 19:1404-1407
Kimura disease (KD) is an autoimmune eosinophilic granulomatous disorder with generalized lymphadenopathy. A handful of pediatric patients with renal disease have been described, none of whom have been African-American (AA). We present an AA boy with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18e31dea96c96f5e27c2ba94cfe16fef
https://doi.org/10.1007/s00467-004-1593-y
https://doi.org/10.1007/s00467-004-1593-y
Publikováno v:
Pediatric Nephrology. 19:738-743
Systemic lupus erythematosus (SLE) tends to be severe and to have a variable response in childhood. We undertook this retrospective study to assess response rates and outcome in 14 children with SLE. Mean age at onset was 12.8+/-3.1 years. Ten patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48bcf19b35e303809c7ea7237ffab83d
https://doi.org/10.1007/s00467-004-1496-y
https://doi.org/10.1007/s00467-004-1496-y
Autor:
Darren J. Day, Dianne Webster, Naznin Dixit, Toni Torresani, Phyllis W. Speiser, Jodene Fitness, Robert Pergolizzi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 84:960-966
We investigated the feasibility and diagnostic utility of genotyping 9 CYP21 mutations, linked chromosome 6p markers, and a dimorphic X-Y marker from neonatal screening samples. Blood-impregnated filter papers (Guthrie cards) from 603 randomly chosen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e0bef9e69ef5841569e8dd84f7decf7
https://doi.org/10.1210/jcem.84.3.5550
https://doi.org/10.1210/jcem.84.3.5550
Autor:
Naznin Dixit, Naveen Uli, Phyllis W. Speiser, Raphael David, Julianne Imperato-McGinley, Daisy Chin, Sharon E. Oberfield
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:1940-1945
We sought to determine the concordance of the phenotype and genotype in a kindred with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The variation in phenotypic expression within this family underscores the difficulty of es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5fcbe1516f1629d8223c4217ad3dcc1
https://doi.org/10.1210/jcem.83.6.4887
https://doi.org/10.1210/jcem.83.6.4887