Results 81 to 90 of about 1,147,373 (216)

Cowden syndrome - Diagnostic skin signs [PDF]

, 2001
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast cancer. The most important clinical features include carcinomas of the breast and thyroid, and hamartomatous polyps of the gastrointestinal tract.
Burgdorf, Walter H. C., Hildenbrand, C., Lautenschlager, Stephan, S. Lautenschlager, C. Hildenbrand, W.H.C. Burgdorf   +5 more
core   +1 more source

Musculoskeletal decay and bone–muscle crosstalk during physical disuse: Mechanisms and integrated countermeasures

Experimental Physiology, EarlyView.
Abstract Older adults experience a markedly increased risk of falls and fractures following hospital discharge, largely due to the rapid musculoskeletal deterioration associated with bed rest. Although age‐related muscle and bone loss typically develops gradually, acute physical inactivity accelerates key biological processes underlying sarcopenia and ...
Julia Margarita Reyes, Guy Hajj‐Boutros, Dounia Rouabhia, José Morais, Felipe Salech, Gustavo Duque   +5 more
wiley   +1 more source

Atypical Reye syndrome: three cases of a problem that pediatricians should consider and remember. [PDF]

Acta Biomed, 2021
Ferretti S, Gatto A, Curatola A, Pansini V, Graglia B, Chiaretti A.   +5 more
europepmc   +1 more source

Reye syndrome

, 1999
Обговорюються результати З секційних спостережень синдрому Рея у дітей. У всіх випадках діагноз встановлено на основі даних секційного спостереження.
Дейнека, С. В., Шатрова, К. М., Заяц, Е. Г.   +2 more
core  

Translating cardiovascular ion channel and Ca2+ signalling mechanisms into therapeutic insights

The Journal of Physiology, EarlyView.
Abstract figure legend This white paper integrates mechanistic discoveries across ion channel biology, Ca2+ signalling and multiscale cardiovascular physiology to highlight new opportunities for accelerating research and guiding next‐generation therapies. Printed with permission from ®Anita Impagliazzo Medical Illustration. [Correction added on 2 March
Silvia Marchianò, Miguel Martín‐Aragón Baudel, Charlotte E. R. Smith, Gonzalo Hernandez Hernandez, Donald M. Bers, Patrick M. Boyle, Dobromir Dobrev, Shanna Hamilton, Osama F. Harraz, Na Li, Thomas A. Longden, William E. Louch, Madeline Nieves‐Cintron, Matthew A. Nystoriak, Walter Lee Murfee, Przemysław B. Radwański, Swapnil K. Sonkusare, Manuel F. Navedo, Eleonora Grandi   +18 more
wiley   +1 more source

A different perspective into clinical symptoms in CPT I deficiency

Molecular Genetics and Metabolism Reports
Carnitine palmitoyltransferase I (CPT I) deficiency is an autosomal recessive disorder causing long-chain fatty acid oxidation defect, characterized by metabolic decompensation episodes accompanied by hypoketotic hypoglycemia, hepatomegaly, seizures ...
Mehmet Cihan Balci, Meryem Karaca, Arzu Selamioglu, Huseyin Kutay Korbeyli, Asli Durmus, Belkis Ak, Tugba Kozanoglu, Gulden Fatma Gokcay   +7 more
doaj   +1 more source

Le syndrome de Reye

, 2012
Le syndrome de Reye est défini comme une encéphalopathie inexpliquée chez les enfants de moins de seize ans, associée à des taux sériques de transaminases et/ou d'ammonium plasmatique supérieurs à trois fois la normale, avec une infiltration lipidique du
GRESSIER, Bernard, MESKINI, Sabah
core  

Glial Dysfunction and Memory Impairments in a Model of Pediatric Obstructive Sleep Apnea

Glia, Volume 74, Issue 11, November 2026.
Generation and analysis of an snRNA‐seq atlas of the hippocampus in POSA. Validation of reduced protein expression of six genes across four cell types. Cellular‐level investigation of aberrant glial function in POSA using transgenic reporter mice. ABSTRACT Pediatric obstructive sleep apnea (POSA) is a common childhood disease that often causes aberrant
Michael R. Williamson, Jorge Botas, Mahyar J. Hedayatpour, Thea Zlatkov, Akdes Serin Harmanci, Christopher J. Yates, Kenneth Nobleza, Roshan Ailani, Adam C. Adler, Farrah Kheradmand, Hyun Kyoung Lee, Benjamin Deneen, Hyun‐Hwan Jeong, Arvind Chandrakantan   +13 more
wiley   +1 more source

Reye, Raimund (1903–1968), and Reubena Emily (Thompson, 1899–1992)

, 2020
Raimund and Reubena Reye worked as missionaries among the Samoan people in Samoa in the 1920s through the 1940s. Raimund Reye was the principal of the West Australian Missionary College for 14 years in the 1950s and 1960s.
Hook, Milton
core   +2 more sources

Aspirin as a Risk Factor in Reye\u27s Syndrome

, 1982
Fifty-six cases of Reye\u27s syndrome (RS) in school-aged children were reported in Michigan during the winter of 1979-1980. The parents of 25 of these children were interviewed in the spring of 1980, as were controls matched to the cases for age, race ...
Hall, William N., Waldman, Ronald J., Van Amburg, George, Mcgee, Harry   +3 more
core   +1 more source