Results 71 to 80 of about 5,631,965 (202)
MedComm, Volume 7, Issue 9, September 2026.Mitochondria is the hub of apoptosis in various diseases. The disruption of mitochondrial structure (including membrane rupture, cristae remodeling, and mitochondrial membrane lipid redistribution), the imbalance of mitochondrial dynamics (including fusion and fission, autophagy), the release, disruption, and mutation of mitochondria DNA, as well as ...
Rubin Tan +9 more
wiley +1 more source
Masive enterorrhagia in patients suffering from hippel-lindau disease
Acta Médica del Centro, 2008 The Von Hippel Lindau disease is an autosomic-dominant neoplasia syndrome produced by a delection or mutation of tumor suppressor gene of chromosome 3p25. It was descripted by the German pathologist Arvid Lindau and the ophthalmologist Eugene Von Hippel,
Jorge Luis González Jara +2 more
doaj
Long‐term outcomes and repeat percutaneous cryoablation in hereditary RCC: a EuRECA cohort
BJU International, EarlyView.
Jens Borgbjerg +16 more
wiley +1 more source
Enfermedad de Von Hippel-Lindau: una presentación atípica [PDF]
, 2004 OBJETIVO: Describir una presentación atípica de la enfermedad de von Hippel-Lindau. MATERIAL Y MÉTODO: Presentamos la clínica, diagnóstico y tratamiento de las manifestaciones urológicas de esta enfermedad, de índole mayormente neurológica, en un varón ...
Murio,E. +9 more
core +1 more source
A case of von Hippel-Lindau disease with exudative maculopathy
Oman Journal of Ophthalmology, 2009 Von Hippel-Lindau (VHL) disease is a rare multisystem familial tumor syndrome of autosomal dominant inheritance. Hallmark lesions include retinal, cerebellum and spinal cord hemangioblastomas, renal cell carcinomas, adrenal pheochromocytomas, angiomatous
Basel T Ba′arah
doaj +3 more sources
Urologic implications of von Hippel-Lindau syndrome
Urology, 1978 A patient with von Hippel-Lindau syndrome is presented. Bilateral simultaneous radical nephrectomy was performed for bilateral renal cell carcinoma without evidence of metastasis. The literature is reviewed and the urologic implications of this syndrome are emphasized.
From the Department of Surgery (Urology), University of Florida College of Medicine, Gainesville, Florida, USA ( host institution ) +1 more
openaire +3 more sources
, 1976 Von Hippel Lindau Disease with a mini retinal tumor. Pair with R1_C4b. Anatomy: Retina. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau disease. Clinical: No visual symptoms. Imaging: Flourescien angiogram in R1_C4b.IC-E2ciii-von-hippel-
William F. Hoyt, MD
core
Von Hippel-Lindau syndrome from the urologist and oncologist perspective — literature review
Oncology in Clinical PracticeVon Hippel-Lindau (VHL) syndrome is a rare genetic disorder characterized by multiple retinal and cerebellar hemangioblastomas that tend to occur in a familial setting. The pattern of inheritance is autosomal dominant.
Krzysztof Kowalik +8 more
doaj +1 more source
Compounds for treating Von Hippel-Lindau disease
, 2018 [EN] The invention relates to the use of a selective 2 adrenergic receptor antagonist for treating and preventing a tumor in a patient with von Hippel-Lindau syndrome.
Albiñana, Virginia +2 more
core