Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sarina Koilpillai"'
Autor:
Mohammed Omar Al Salihi, Murali K Iyyani, Sarina Koilpillai, Gerson Quintero, Jorge Parellada, SJ Carlan
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Multiple endocrine neoplasia 2A is an autosomal dominant disease characterized by medullary thyroid cancer, pheochromocytoma, and primary hyperparathyroidism. Coronary artery disease is associated with the disorder, but the mechanism is unclear. A 27
Externí odkaz:
https://doaj.org/article/795c1d54d56242ae876cb58b258b27fa
Publikováno v:
Case Reports in Medicine, Vol 2022 (2022)
Background. Clinical B12 deficiency with hematological or neurological manifestations is rare. An unusual manifestation of B12 deficiency is pseudo-thrombotic microangiopathy (TMA), which is characterized by hemolytic anemia, thrombocytopenia, and sc
Externí odkaz:
https://doaj.org/article/e1e4c32108204e40b86eb9f52c3aa26e
Publikováno v:
European Journal of Clinical Medicine. 4:1-3
Morbid obesity is a major health problem worldwide and the Roux-en-Y gastric bypass (RYGB) is a popular surgical treatment. A 40 year old woman, 17 years post RYGB presented with concurrent symptomatic gastric ulcers and acute pancreatitis. The diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d9740de92949cdaef07c46e50d1f41c
https://doi.org/10.24018/clinicmed.2023.4.2.241
https://doi.org/10.24018/clinicmed.2023.4.2.241
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24b4a8cb9075082c50809ea42e683b07
https://doi.org/10.7759/cureus.37430
https://doi.org/10.7759/cureus.37430
Autor:
Sarina Koilpillai, Thomas Y. Sun, Jacqueline Kropf, Mario Madruga, Sanobar Yasmeen Mohammed, Steve J. Carlan
Publikováno v:
The American journal of case reports. 23
BACKGROUND Primary retroperitoneal choriocarcinoma is a rare form of extragonadal germ cell tumor that is highly aggressive and responds poorly to chemoradiation. Extragonadal choriocarcinomas are notoriously challenging to diagnose, and have often p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b95ac07e73bd847caaa58267fbd15b75
https://pubmed.ncbi.nlm.nih.gov/35927927
https://pubmed.ncbi.nlm.nih.gov/35927927
Publikováno v:
BMJ case reports. 15(6)
Immune thrombocytopenic purpura (ITP) is an autoimmune disorder caused by autoantibodies against platelet antigens resulting in platelet destruction and inhibition of platelet production. Occasionally, an inciting event such as a virus or vaccination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d899c1cc83b36c3ae8e0a62d121ba5f
https://pubmed.ncbi.nlm.nih.gov/35725277
https://pubmed.ncbi.nlm.nih.gov/35725277
Autor:
Bianca, Dominguez, Sarina, Koilpillai, Omar, Qazi, Gerson, Quintero, Mario, Madruga, Steve J, Carlan
Publikováno v:
American Journal of Case Reports. 23
BACKGROUND Neuromyelitis optica (NMO) is a rare neurological disease characterized by attacks of transverse myelitis and optic neuritis, contiguous spinal cord lesions on more than 3 vertebral segments on magnetic resonance imaging (MRI), and seropos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6d5693ced16fed8c52e69809179d0b
https://doi.org/10.12659/ajcr.936283
https://doi.org/10.12659/ajcr.936283