Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Shailesh B. Patel"'
Autor:
Ancuta Muntean, Ramona Cazacu, Niyi Ade-Ajayi, Shailesh B Patel, Kypros Nicolaides, Mark Davenport
Publikováno v:
Journal of pediatric surgery.
Insertion of a thoraco amniotic shunt (TAS) during fetal life is a therapeutic option where there is a high risk of death secondary to large congenital lung malformations (CLM). The aim of this study is to present our center's long-term experience.Re
Autor:
Apurva More, Shailesh B. Patel
Publikováno v:
Handbook of Pediatric Surgery ISBN: 9783030844660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26c9959d22c161e54da7b7321f25628f
https://doi.org/10.1007/978-3-030-84467-7_9
https://doi.org/10.1007/978-3-030-84467-7_9
Autor:
Ancuta Muntean, Liliana-Elena Banias, Niyi Ade-Ajayi, Shailesh B. Patel, Olivia McKinney, Mark Davenport
Publikováno v:
Journal of pediatric surgery. 57(11)
Congenital pulmonary airway malformation (CPAM) has an estimated prevalence in Europe of 1.06/10,000 live births with most being detected using maternal ultrasound screening. Malignant transformation is a possible complication though its prevalence i
Publikováno v:
European Heart Journal. 41:2629-2631
Autor:
Shailesh B. Patel, Hongwei Yu, Gerald Salen, Mi Hye Lee, Jianling Chen, Bhaswati Pandit, Eric L. Klett, Gwang Sook Anh
Publikováno v:
International Congress Series. 1262:300-304
Investigation and study of rare genetic disorders can lead to considerable and rapid advancements into understanding common and basic physiological processes. One such case is the study of the rare human disorder of sitosterolemia. This autosomal rec
Autor:
Vinaya Simha, Alyne Ricker, Lihadh Al-Gazali, Neil H. White, Kurt A. Kennel, Karen L. Herbst, Aharon Klar, Figen Gürakan, Silva A. Arslanian, Anil K. Agarwal, Zohra Zaidi, Phillip Gorden, L. Bindl, Abhimanyu Garg, Elif A. Oral, Shailesh B. Patel, Stephanie Ann Moran, Stephen O'Rahilly
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 88:4840-4847
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near complete absence of adipose tissue from birth. Recently, mutations in 1-acylglycerol-3-phosphate O-acyltransferase 2 (AGPAT2) and Berardinelli-Sei
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 7, Pp 1277-1288 (1997)
Scopus-Elsevier
Scopus-Elsevier
Dyslipidemia secondary to obesity is commonly observed in both animals and humans. As it has been hypothesized that obesity can result in overproduction of VLDL, leading to the subsequent dyslipidemia, we have examined the triglyceride and apoB secre
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 32
We report a family with extremely depressed high density lipoprotein (HDL) cholesterol (C) levels. The proband, a 27 year-old male of Asian Indian origin, was identified on routine lipid screening to have an HDL-C of 9mg/dL. His 24 year-old brother h
Autor:
Shailesh B. Patel
Publikováno v:
Handbook of Pediatric Surgery ISBN: 9781848821316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3603d38dcca57fa4797f0a639d77a939
https://doi.org/10.1007/978-1-84882-132-3_59
https://doi.org/10.1007/978-1-84882-132-3_59
Autor:
Eric L, Klett, Shailesh B, Patel
Publikováno v:
Science (New York, N.Y.). 303(5661)