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pro vyhledávání: '"ASHIM AHUJA"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 5, Pp TD06-TD08 (2015)
Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract resulting from maldevelopment of both Mullerian and Wolffian ducts. It is characterized by the triad of uterus didelphys, obstructed hemivagina and ips
Externí odkaz:
https://doaj.org/article/93deb96128194ad1830348d764d37e39
Autor:
Ashim Ahuja
Publikováno v:
Journal of the Endocrine Society
Objective To report a case in which Cabergoline led to pituitary apoplexy (PA) in a young female patient with a macroprolactinoma. Methods A 28 y/o F presented with 10 months of irregular menses followed by 6 months of amenorrhea. She reported a dull
Autor:
Julie A. Schneider, Zhen Zhao, Qingyi Ma, Ethan A. Winkler, Anita Ramanathan, Takahiro Maeda, Ashim Ahuja, Justin K. Ichida, Carol A. Miller, Pan Kong, Matthew R. Halliday, Guojun Bu, Takahisa Kanekiyo, Sanket V Rege, Manami Maeda, Tohru Sugawara, Berislav V. Zlokovic, Donghui Zhu, Kassandra Kisler, Abhay P. Sagare, Nelly Chuqui Owens, Gabriel Si
Publikováno v:
Nature neuroscience
PICALM is a highly validated genetic risk factor for Alzheimer's disease (AD). We found that reduced expression of PICALM in AD and murine brain endothelium correlated with amyloid-β (Aβ) pathology and cognitive impairment. Moreover, Picalm deficie
Autor:
Anita Ramanathan, Yi Zhou, Divna Lazic, Amy R. Nelson, Ashim Ahuja, Philbert S. Tsai, Berislav V. Zlokovic, Yaoming Wang, David A. Boas, Kassandra Kisler, Sava Sakadžić, Zhen Zhao, Sanket V Rege
Publikováno v:
Nature neuroscience
Pericytes are perivascular mural cells of brain capillaries that are positioned centrally within the neurovascular unit between endothelial cells, astrocytes and neurons. This unique position allows them to play a major role in regulating key neurova
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 5, Pp TD06-TD08 (2015)
Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract resulting from maldevelopment of both Mullerian and Wolffian ducts. It is characterized by the triad of uterus didelphys, obstructed hemivagina and ipsi