Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Minal Wade"'
Publikováno v:
Indian Journal of Community Medicine, Vol 44, Iss 2, Pp 152-156 (2019)
Introduction: Anemia has been widely reported to predict a poorer prognosis for HIV-infected patients, both in terms of progression to AIDS and in survival. This study aimed to determine the etiology of anemia and its immunological correlation in HIV
Externí odkaz:
https://doaj.org/article/d81e8d305adb4946a738b1e00ff465f3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp SD04-SD06 (2017)
Systemic hyalinosis is inherited as an autosomal recessive disease. It may also be referred to as Fibromatosis hyalinica multiplex juvenilis and Murray-Puretic-Drescher syndrome. A four and a half-year-old female child presented with multiple soft t
Externí odkaz:
https://doaj.org/article/e77600b814a242e3b96dba01910202d6
Publikováno v:
Pediatric Oncall. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c42996632625c6b341122922f999510a
https://doi.org/10.7199/ped.oncall.2025.30
https://doi.org/10.7199/ped.oncall.2025.30
Publikováno v:
GLOBAL JOURNAL FOR RESEARCH ANALYSIS. :1-2
Background:1 Langerhans cell histiocytosis (LCH) is characterized by monoclonal proliferation and inltration of organs by Langerhans cell. Pulmonary involvement is common in young adults, but it is uncommon in children. Case summary: A 7 month old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cfc665fa9487f47b6f70957fdbb0384
https://doi.org/10.36106/gjra/6900647
https://doi.org/10.36106/gjra/6900647
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp SD04-SD06 (2017)
Systemic hyalinosis is inherited as an autosomal recessive disease. It may also be referred to as Fibromatosis hyalinica multiplex juvenilis and Murray-Puretic-Drescher syndrome. A four and a half-year-old female child presented with multiple soft ti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577d94516b3289761ee7022edef00fd9
https://doi.org/10.7860/jcdr/2017/25280.10293
https://doi.org/10.7860/jcdr/2017/25280.10293
Publikováno v:
International Journal of Research in Medical Sciences. 7:3993
Background: Errors in sampling during blood culture, may lead to contaminants or poor yield which result in faulty reports increasing patient's suffering, endanger patient safety and increasing cost of health care. Optimal knowledge about the samplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24259ccc1e019bfc85faab3c30aa9ce7
https://doi.org/10.18203/2320-6012.ijrms20194642
https://doi.org/10.18203/2320-6012.ijrms20194642
Publikováno v:
International Journal of Research in Medical Sciences. 7:4361
In children with gross, persistent ascites wherein clinical scenario is not agreeable to common conditions, one needs to revise the diagnosis and rule out the surgical cause for abdominal distension mimicking ascites. We are reporting here, a case of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d90a7da12578a0f719c36dd14efd5a82
https://doi.org/10.18203/2320-6012.ijrms20194644
https://doi.org/10.18203/2320-6012.ijrms20194644
Publikováno v:
International Journal of Research in Medical Sciences. 7:4396
Protein Losing Enteropathy Post Fontan procedure. Protein Losing Enteropathy (PLE) is an uncommon cause of edema in children with congenital heart disease. Protein-Losing Enteropathy may be defined as excessive loss of proteins across the intestinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0032b5669c76475dbabc0d263d866f7
https://doi.org/10.18203/2320-6012.ijrms20194623
https://doi.org/10.18203/2320-6012.ijrms20194623
Autor:
Chandra Kiran Chunchu, Charusheela Sujit Korday, Priyanka Modi, Dinesh Singh, Baraturam Bhaisara, Minal Wade
Publikováno v:
International Journal of Contemporary Pediatrics. 6:2712
Transient leukemia of Down syndrome(TL-DS) or transient myeloproliferative disorder (TMD) or transient abnormal myelopoiesis (TAM) is a hematologic abnormality characterized by an uncontrolled proliferation of myeloblasts in peripheral blood and bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2534bcb5f2697982f63e8310a86b0db
https://doi.org/10.18203/2349-3291.ijcp20194615
https://doi.org/10.18203/2349-3291.ijcp20194615
Autor:
Anupama Mauskar, Anjali M. Bhatawdekar, Minal Wade, Baraturam Bhaisara, Vikram V. Yaragatti, Charusheela Sujit Korday
Publikováno v:
International Journal of Contemporary Pediatrics. 6:2671
Intrauterine thrombosis with extremity ischemia presenting at birth in a newborn is a rare event. A 29 year old mother, 2nd gravida with one first trimester spontaneous abortion delivered a 33week gestation male preterm baby. On Examination, the enti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7428de5ca430379359f5e64d505634cf
https://doi.org/10.18203/2349-3291.ijcp20194538
https://doi.org/10.18203/2349-3291.ijcp20194538