Results 141 to 150 of about 50,269 (341)

The efficacy of topical treatments for acanthosis nigricans: a systematic review of randomized controlled trials

Frontiers in Medicine
BackgroundAcanthosis nigricans (AN) is a skin disorder marked by darkening and thickening of the skin, often linked to metabolic abnormalities. This systematic review of randomized controlled trials (RCTs) assesses the comparative effectiveness and ...
Awadh Alamri, Awadh Alamri, Awadh Alamri, Rose A. Alraddadi, Rose A. Alraddadi, Dhaii Alzahrani, Dhaii Alzahrani, Amal H. Abualola, Hadeel A. Maaddawi, Renad F. Alharthy, Renad F. Alharthy, Alanoud Y. Alkhashan, Maria Y. Ashqan, Esraa A. Shaheen, Bashaer Almahdi, Hatoon M. Althobaiti   +15 more
doaj   +1 more source

Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndrome. [PDF]

, 1994
Jeanette C. Ramer, D B Vasily, Roger L. Ladda   +2 more
openalex   +1 more source

Cutaneous non‐tuberculous mycobacterial infections: A retrospective study of 94 cases from Germany

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background Cutaneous non‐tuberculous mycobacterial infections (NTM) remain a diagnostic and therapeutic challenge. The aim of this study was to characterize cutaneous NTM infections in Germany over a 24‐year‐period. Patients and Methods 73 patients with cutaneous NTM infections diagnosed at 17 different German University Hospitals from 2000 ...
Luisa Bopp, Nicolai Deresz, Henning Klapproth, Isabelle Suárez, Jonathan Jantsch, Mario Fabri, Esther von Stebut   +6 more
wiley   +1 more source

Palmer plantar hyperkeratosis--a previously undescribed skin manifestation of juvenile dermatomyositis [PDF]

, 1997
Y. See, Madeleine Rooney, P Woo
openalex   +1 more source

Unilateral nipple hyperkeratosis [PDF]

JAAD Case Reports, 2019
Gregory R. Delost, Jeffrey F. Scott, Timmie R. Sharma, Nehal Shah   +3 more
openaire   +3 more sources

Papillon-Lefevre Syndrome

Česká Stomatologie a Praktické Zubní Lékařství, 2009
Papillon-Lefevre syndrome (PLS) is a rare autosomal recessive disorder characterized by severe early-onset periodontal destruction involving both the deciduous and permanent dentition and skin lesions of palmoplantar hyperkeratosis. Recently it was found
L. Izakovičová Hollá, A. Fassmann, M. Kukletová, V. Sazmová   +3 more
doaj  

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350) [PDF]

, 2000
Kirsten Heathcote
openalex   +1 more source

Pathogenesis and management of TRPV3-related Olmsted syndrome

Frontiers in Genetics
Olmsted syndrome is characterized by symmetrically distributed, destructive, inflammatory palmoplantar keratoderma with periorificial keratotic plaques, most commonly due to gain-of-function mutations in the transient receptor potential vanilloid 3 ...
Antong Lu, Antong Lu, Antong Lu, Antong Lu, Kezhen Li, Kezhen Li, Kezhen Li, Kezhen Li, Cong Huang, Cong Huang, Cong Huang, Bo Yu, Bo Yu, Bo Yu, Bo Yu, Bo Yu, Weilong Zhong, Weilong Zhong, Weilong Zhong   +18 more
doaj   +1 more source

Hyperkeratosis in Response to Mechanical Irritation**From the Section of Dermatology, School of Medicine, University of Chicago, Chicago, Illinois (Chief of Service: Stephen Rothman, M.D.)

, 1949
Louis Rubin
openalex   +1 more source

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis [PDF]

, 2017
Epidermolytic hyperkeratosis (EHK) is a blistering skin disease inherited as an autosomal-dominant trait. The disease is caused by genetic defects of the epidermal keratin K1 or K10, leading to an impaired tonofilament network of differentiating ...
Arin, Meral J., Hausser, Ingrid, Hohl, Daniel, Huber, Marcel, Kinaciyan, Tamar, Korge, Bernhard P., Krieg, Thomas, Müller, Felix B., Schaffrath, Christina   +8 more
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