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Longer titles found: Dennie–Marfan syndrome (view)

searching for Marfan syndrome 31 found (281 total)

Pauline de Rothschild (1,905 words) [view diff] no match in snippet view article find links to article

Pauline, Baroness de Rothschild (née Potter; December 31, 1908 – March 8, 1976) was an American fashion designer, writer and, with her second husband,

Charles Clayton Dennie (177 words) [view diff] exact match in snippet view article find links to article

Dennie (1883–1971) was an American dermatologist, notable for Dennie-Marfan syndrome and Dennie-Morgan fold. Charles Clayton Dennie was born in Excelsior

Kenshi Yonezu (3,978 words) [view diff] no match in snippet view article find links to article

Kenshi Yonezu (米津玄師, Yonezu Kenshi) is a Japanese musician, singer-songwriter, record producer and illustrator who began releasing Vocaloid music under

Merzbox (4,252 words) [view diff] case mismatch in snippet view article find links to article

Akita – EMS Synthi 'A', noise electronics, metal, filters, voice "Marfan Syndrome for Blue" is Akita's first track to use the EMS synthesiser. Track

Lizzie Velásquez (1,553 words) [view diff] exact match in snippet view article find links to article

Gillesen-Kaesbach G, Fahsold R, Schmidt H, Hoffmann K, Passarge E (2010). "Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with

Acne fulminans (939 words) [view diff] exact match in snippet view article find links to article

H.; Koch, A.; Köstler, E. (2005). "Case reports: acne fulminans in Marfan syndrome". J Drugs Dermatol. 4 (4): 501–5. ISSN 1545-9616. PMID 16004026. Zaba

Degenerative disease (1,614 words) [view diff] exact match in snippet view article find links to article

F; Hui, R; Zhou, X (2010). "Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders". Ageing Research Reviews. 9 (3): 363–368

Wiedemann–Rautenstrauch syndrome (761 words) [view diff] exact match in snippet view article find links to article

P, de Paepe A, et al. (April 2014). "Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end

Myosin-11 (1,334 words) [view diff] exact match in snippet view article find links to article

inherited in isolation or in association with genetic syndromes, such as Marfan syndrome and Loeys-Dietz syndrome. When TAAD occurs in the absence of syndromic

Popliteal artery aneurysm (549 words) [view diff] exact match in snippet view article find links to article

tobacco smoking, atherosclerosis, connective tissue disorders (e.g. Marfan syndrome, and Ehlers-Danlos syndrome), advanced age (peaking in the 6th to 7th

Oligogenic inheritance (1,121 words) [view diff] case mismatch in snippet view article find links to article

Chen, Harold (11 January 2021). Buehler, Bruce (ed.). "Genetics of Marfan Syndrome". Medscape. WebMD LLC. Stafford, Kate; Mannor, Michael. "Mutations

ASHG Scientific Achievement Award (762 words) [view diff] case mismatch in snippet view article find links to article

doi:10.1086/500330. PMC 1559547. PMID 16909379. Dietz, H. C. (2007). "Marfan Syndrome: From Molecules to Medicines". The American Journal of Human Genetics

Alana Cordy-Collins (512 words) [view diff] exact match in snippet view article find links to article

averaged between 4-foot-10 and 5-foot-6. The noblemen suffered from Marfan syndrome, an inherited form of gigantism. These are the first recorded instances

Transforming growth factor (596 words) [view diff] exact match in snippet view article find links to article

HC (Aug 2009). "Circulating transforming growth factor-{beta} in Marfan syndrome". Circulation. 120 (6): 526–32. doi:10.1161/CIRCULATIONAHA.108.841981

FBLN2 (1,268 words) [view diff] exact match in snippet view article find links to article

"Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2" (PDF). Eur. J. Hum. Genet. 4 (5): 292–5. doi:10.1159/000472216

Robert King Stone (595 words) [view diff] case mismatch in snippet view article find links to article

planning.dc.gov Boritt, Gabor S.; Borit, Adam (1983). "Lincoln and the Marfan Syndrome: The Medical Diagnosis of a Historical Figure". Civil War History.

Decorin (1,949 words) [view diff] exact match in snippet view article find links to article

"Deficient expression of the gene coding for decorin in a lethal form of Marfan syndrome". The Journal of Biological Chemistry. 265 (29): 17780–5. doi:10

Beta blocker (7,102 words) [view diff] exact match in snippet view article find links to article

use of beta blockers to prevent aortic dissections in people with Marfan syndrome was unable to draw definitive conclusions due to lack of evidence.

Human genetics (2,444 words) [view diff] case mismatch in snippet view article find links to article

(SDSC). Chen, Harold (2019-03-08). Buehler, Bruce (ed.). "Genetics of Marfan Syndrome". Medscape. WebMD LLC. Stafford, Kate; Mannor, Michael. "Mutations

Clair Francomano (828 words) [view diff] exact match in snippet view article find links to article

Stetten, Gail; Meyers, Deborah A.; Francomano, Clair A. (July 1991). "Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene"

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (1,459 words) [view diff] exact match in snippet view article find links to article

signaling is involved in causing CARASIL. This approach has been used in Marfan syndrome, which also involves excessive TGF-β signaling. This suggestion has

LRP1 (3,564 words) [view diff] exact match in snippet view article find links to article

of TGFbeta and PDFG signals in the vascular wall: implications for Marfan syndrome". PLOS ONE. 2 (5): e448. Bibcode:2007PLoSO...2..448B. doi:10.1371/journal

Goldberg–Shprintzen syndrome (1,327 words) [view diff] exact match in snippet view article find links to article

Goldberg–Shprintzen syndrome, a number of these genetic tests also test for Marfan syndrome and other syndromes closely related to Goldberg–Shprintzen syndrome

Candidate gene (2,679 words) [view diff] exact match in snippet view article find links to article

"Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome". Brazilian Journal of Medical and Biological Research. 44 (8): 793–800

Aneurysm (5,367 words) [view diff] exact match in snippet view article find links to article

infection.: 602 Connective tissue disorders such as Loeys-Dietz syndrome, Marfan syndrome, and certain forms of Ehlers-Danlos syndrome are also associated with

Aortic valve replacement (4,504 words) [view diff] exact match in snippet view article find links to article

aortic root dilatation, trauma, connective tissue disorders such as Marfan syndrome or Ehlers-Danlos lead to imperfect closure of the valve during diastole

Progeroid syndromes (8,724 words) [view diff] exact match in snippet view article find links to article

Gillesen-Kaesbach G, Fahsold R, Schmidt H, Hoffmann K, Passarge E (2010). "Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with

Masami Akita discography (581 words) [view diff] case mismatch in snippet view article find links to article

Paradise "Twisted Domiano" Cataclastic Fracture Deadline and Lazy Squid "Marfan Syndrome for Blue" Eternal Blue Extreme: An Asian Tribute to Derek Jarman Somnus

Steve Wilton (1,837 words) [view diff] exact match in snippet view article find links to article

splice-switching antisense oligomers in addressing various diseases such as Marfan syndrome and juvenile-onset Parkinson's disease. His earlier research identified

Maternal mortality in the United States (9,582 words) [view diff] case mismatch in snippet view article find links to article

heart disease, vascular aneurysm, hypertensive cardiovascular disease, Marfan Syndrome, conduction defects, vascular malformations, and other cardiovascular

Physical oncology (6,734 words) [view diff] exact match in snippet view article find links to article

"Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome". Journal of Clinical Investigation. 124 (3): 1329–39. doi:10.1172/jci71059