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Akademický článek

Optical coherence tomography angiography of astrocytic hamartoma demonstrates intrinsic vascularity

Autor: Ryan N. Vogel, T.Y. Alvin Liu, Mandeep S. Singh, Morton F. Goldberg

Publikováno v: American Journal of Ophthalmology Case Reports, Vol 20, Iss , Pp 100924- (2020)

Purpose: To evaluate the findings of astrocytic hamartoma in the setting of gyrate atrophy, including details of optical coherence tomography angiography (OCTA). Observations: Multimodal imaging was obtained on a 20-year-old woman with genetically-co

Externí odkaz: https://doaj.org/article/fe805ea162ea457d8116f81592889d85

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Akademický článek

Expression of the angiogenic mediator, angiopoietin-like 4, in the eyes of patients with proliferative sickle retinopathy.

Autor: Kathleen Jee, Murilo Rodrigues, Fabiana Kashiwabuchi, Brooks P Applewhite, Ian Han, Gerard Lutty, Morton F Goldberg, Gregg L Semenza, Silvia Montaner, Akrit Sodhi

Publikováno v: PLoS ONE, Vol 12, Iss 8, p e0183320 (2017)

The recent success of therapies directly targeting the angiogenic mediator, vascular endothelial growth factor (VEGF), for the treatment of proliferative diabetic retinopathy has encouraged clinicians to extend the use of anti-VEGF therapies for the

Externí odkaz: https://doaj.org/article/022e349caace4b2b823cf5d9db7a4533

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Akademický článek

Mutant SOD1 forms ion channel: Implications for ALS pathophysiology

Autor: Michael J. Allen, Jérome J. Lacroix, Srinivasan Ramachandran, Ricardo Capone, Jenny L. Whitlock, Ghanashyam D. Ghadge, Morton F. Arnsdorf, Raymond P. Roos, Ratnesh Lal

Publikováno v: Neurobiology of Disease, Vol 45, Iss 3, Pp 831-838 (2012)

Point mutations in the gene encoding copper–zinc superoxide dismutase (SOD1) impart a gain-of-function to this protein that underlies 20–25% of all familial amyotrophic lateral sclerosis (FALS) cases. However, the specific mechanism of mutant SOD

Externí odkaz: https://doaj.org/article/1e5212b449004cdd8c77cbbfb81a3e01

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Akademický článek

Erratum to 'Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease: An Update on Management'

Autor: Samir K. Ballas, Muge R. Kesen, Morton F. Goldberg, Gerard A. Lutty, Carlton Dampier, Ifeyinwa Osunkwo, Winfred C. Wang, Carolyn Hoppe, Ward Hagar, Deepika S. Darbari, Punam Malik

Publikováno v: The Scientific World Journal, Vol 2013 (2013)

Externí odkaz: https://doaj.org/article/d761f4b513cc4d40ad0787903955f7e8

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Akademický článek

Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease: An Update on Management

Autor: Samir K. Ballas, Muge R. Kesen, Morton F. Goldberg, Gerard A. Lutty, Carlton Dampier, Ifeyinwa Osunkwo, Winfred C. Wang, Carolyn Hoppe, Ward Hagar, Deepika S. Darbari, Punam Malik

Publikováno v: The Scientific World Journal, Vol 2012 (2012)

The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of the β globin gene resulting in the substitution of glutamic acid by valine at position 6 of the β globin polypeptide chain. Although the molecular lesi

Externí odkaz: https://doaj.org/article/df632fd7aa014af895eb7bc31341028a

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