Zobrazeno 1 - 10
of 3 562
pro vyhledávání: '"FH"'
Autor:
Mohammed Abdrabou, Fayez Gebali, Mahmoud A. Shawky, Ala S. Alluhaidan, Ahmed E. Mansour, Sahar A. El-Rahman, Ayman Al-ahwal, Tamer Shamseldin
Publikováno v:
EURASIP Journal on Wireless Communications and Networking, Vol 2024, Iss 1, Pp 1-21 (2024)
Abstract Recently, low Earth orbit (LEO) satellites have emerged as key players in space information network (SIN) due to their ability to provide global coverage. However, they remain susceptible to threats such as denial of service (DoS), man-in-th
Externí odkaz:
https://doaj.org/article/51b7f052aaa54c3382f8180b1cb94451
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare autosomal dominant syndrome caused by a germline mutation in the fumarate hydratase (FH) gene that manifests with cutaneous leiomyomas, uterine fibroids, and renal cell cancer
Externí odkaz:
https://doaj.org/article/0d6d6e25f31145e7b368584e14e30837
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
AimTo study and analyze the clinicopathological features of low-grade fumarate hydratase-deficient renal cell carcinoma in order to improve the understanding of the diagnosis and management of rare and specific morphological cases of this tumor.Metho
Externí odkaz:
https://doaj.org/article/83a0af80d55545959247ed4fa14968e8
Publikováno v:
Frontiers in Surgery, Vol 11 (2024)
BackgroundFumarate hydratase-deficient renal cell carcinoma (FH-RCC) is a rare subtype of kidney tumor. Most of them are solitary lesions, making preoperative diagnosis difficult, aggressive, and with poor prognosis. They may metastasize even at an e
Externí odkaz:
https://doaj.org/article/216df8e9b44242db9e75fac58dc9399a
Autor:
Urte Aliosaitiene, Zaneta Petrulioniene, Egidija Rinkuniene, Antanas Mainelis, Egle Brazdziuniene, Urte Smailyte, Vaida Sileikiene, Aleksandras Laucevicius
Publikováno v:
Lipids in Health and Disease, Vol 23, Iss 1, Pp 1-10 (2024)
Abstract Background Familial hypercholesterolemia (FH) is one of the most common autosomal dominant diseases. FH causes a lifelong increase in low-density lipoprotein cholesterol (LDL-C) levels, which in turn leads to atherosclerotic cardiovascular d
Externí odkaz:
https://doaj.org/article/47af5d75ae8b4174977415e5a92ade82
Publikováno v:
International Journal of Hyperthermia, Vol 41, Iss 1 (2024)
Objective This study aimed to explore the efficacy and safety of high-intensity focused ultrasound (HIFU) ablation for treating fumarate hydratase (FH)-deficient uterine leiomyomas.Method Ten patients with FH-deficient uterine leiomyomas treated with
Externí odkaz:
https://doaj.org/article/f2d6992b1879469993d4de004d33a315
Akademický článek
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Autor:
Jessica S. Kleer, Juliane Klehr, Denise Dubler, Laura Infanti, Carlo Chizzolini, Uyen Huynh-Do, Camillo Ribi, Marten Trendelenburg
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundFactor H (FH) is a major soluble inhibitor of the complement system and part of a family comprising five related proteins (FHRs 1–5). Deficiency of FHR1 was described to be linked to an elevated risk of systemic lupus erythematosus (SLE).
Externí odkaz:
https://doaj.org/article/23c87a1a94b74455bd81117beb17ef42
Autor:
Aseel A. Jawabri, Anne John, Mohammad A. Ghattas, Radwa E. Mahgoub, Mohammad I. K. Hamad, Maha T. Barakat, Bindu Shobi, Hinda Daggag, Bassam R. Ali
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
BackgroundFamilial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by increased LDL-cholesterol levels. About 85% of FH cases are caused by LDLR mutations encoding the low-density lipoprotein receptor (LDLR). LDLR is synthes
Externí odkaz:
https://doaj.org/article/853e9696b4b94268b68dc340efeeb0de
Publikováno v:
Translational Oncology, Vol 45, Iss , Pp 101963- (2024)
Objective: This study presents a detailed analysis of the clinical and genetic characteristics of uterine leiomyoma associated with Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC), combined with exploration of family history, pathology, and m
Externí odkaz:
https://doaj.org/article/7ba20c22347246e296ab5ffc5ec9aac4