Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sujatha Kosuri"'
Publikováno v:
The Journal of Pediatric Pharmacology and Therapeutics. 24:538-541
A case of methemoglobinemia (MHb) in a teenage woman, triggered by an acute ingestion of approximately 120 to 180 mg of cetirizine, allegedly, with no suicidal intent is described. The patient presented with anxiety and tremors and rapidly developed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d14fde9e34e40953bf0a13ff52ef5319
https://doi.org/10.5863/1551-6776-24.6.538
https://doi.org/10.5863/1551-6776-24.6.538
Autor:
Madhuri Penugonda, Dominick Sabatino, Peter Ciminera, Jacob J. Rosenberg, Saumya Sharma, Sujatha Kosuri
Publikováno v:
Challenging Cases in Pediatric Diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cea5142af01947c05a3311335240ad82
https://doi.org/10.1542/9781610020176-part09-ch055
https://doi.org/10.1542/9781610020176-part09-ch055
Autor:
Thomas W. McCloskey, Soo Fang Wang, Sujatha Kosuri, Marianne Frieri, Dominick Sabatino, Gretchen Beck, Paul Cardenas
Publikováno v:
Pediatric Asthma, Allergy & Immunology. 14:239-247
Familial hemophagocytic lymphohistiocytosis (FHLH) is an autosomal recessive disorder associated with hepatosplenomegaly, cytopenias, lymphohistiocytic accumulation in the reticuloendothelial system and hemophagocytosis. Immunological dysregulation c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab349bdaac628d15faa1fac1a41e3161
https://doi.org/10.1089/pai.2000.14.239
https://doi.org/10.1089/pai.2000.14.239
Publikováno v:
Pediatric Hematology and Oncology. 15:447-450
The authors report on 2 children with pernicious anemia, sisters, who presented with hyper-melanosis as one of the clinical manifestations. The hypermelanosis disappeared with adequate treatment of vitamin B12 deficiency. Vitamin Big deficiency shoul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95ad441468f041a275d36f2a1b2c7bb5
https://doi.org/10.3109/08880019809016575
https://doi.org/10.3109/08880019809016575
Autor:
Moris Angulo, Platon J Collipp, Sujatha Kosuri, Janaki Yadlapalli, Boris Espinoza, Mariano Castro-Magana
Publikováno v:
Pediatric Research. 19:194A-194A
504 EARLY PUBERTY IN KLINEFELTER SYNDROME DUE TO A CHORIONIC GONADOTROPIN (hCG)-PRODUCING TUMO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d1e661546201b38fb3d41f7dedb40e8
https://doi.org/10.1203/00006450-198504000-00534
https://doi.org/10.1203/00006450-198504000-00534
Autor:
Mariano Castro-Magana, Jack Sherman, Sujatha Kosuri, Platon J Collipp, Gregory Graworsky, Moris Angulo
Publikováno v:
Pediatric Research. 19:244A-244A
Gaucher disease (GD) is an autosomal recessive condition that presents in a variety of clinical forms, better known as adult, infantile and juvenile or Type 1, 2 and 3 GD respectively. A 22 month old greek female presented with history of progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19957ca517a9bddc907f8490372316cd
https://doi.org/10.1203/00006450-198504000-00829
https://doi.org/10.1203/00006450-198504000-00829