Results 91 to 100 of about 9,543 (240)
Erkennen – Der klinische Blick auf die kutane Tuberkulose
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 793-803, July 2025.Zusammenfassung In vielen Ländern ist die Tuberkulose (TBC) bis heute eine der häufigsten Todesursachen und bleibt insbesondere durch Migrationsbewegungen auch in Deutschland von Bedeutung. Die Diagnose der seltenen kutanen Tuberkulose ist herausfordernd, da sie in vielfältigen klinischen Erscheinungsformen auftritt, die deutlich häufigeren ...
Cathrin Gramminger, Tilo Biedermann
wiley +1 more source
Lyme’i tõve nüüdisaegne diagnostika ja ravi [PDF]
, 2012 Puukborrelioos ehk Lyme’i tõbi (LB) on puukide edasiantav infektsioon, mille tekitajaks on Borrelia burgdorferi. Viimastel aastatel on LB-haigestumus Eestis oluliselt kasvanud.
Lutsar, Irja +2 more
core +2 more sources
Medicine, 2016 Acrodermatitis enteropathica is a rare genetic autosomal recessive disorder, characterized by periorificial dermatitis, alopecia, and diarrhea. It is caused by mutations in the gene that encodes a membrane protein that binds zinc. We report a 14-month-old boy, admitted for erythematous, scaly and pustular lesions, initially located in the inguinal and ...
Nistor, Nicolai +5 more
openaire +2 more sources
United European Gastroenterology Journal, Volume 13, Issue 5, Page 773-797, June 2025.ABSTRACT Malabsorption is a complex and multifaceted condition characterised by the defective passage of nutrients into the blood and lymphatic streams. Several congenital or acquired disorders may cause either selective or global malabsorption in both children and adults, such as cystic fibrosis, exocrine pancreatic insufficiency (EPI), coeliac ...
Marco Vincenzo Lenti +29 more
wiley +1 more source
ACRODERMATITIS ENTEROPATHICA: CLINICAL MANIFESTATIONS AND PEDIATRIC DIAGNOSIS
Revista Paulista de Pediatria, 2018 Objective: To report a case of acrodermatitis enteropathica, a rare disease with autosomal recessive inheritance. Case description: An 11-month-old boy was presenting symmetrical erythematous and yellowish-brownish crusted lesions on his face, feet ...
I. Ciampo +3 more
semanticscholar +1 more source
The Journal of Dermatology, Volume 52, Issue 5, Page 773-786, May 2025.Abstract Secukinumab is one of the human monoclonal antibodies recommended in the Japanese guidelines for patients with psoriasis, but few case reports and clinical studies on secukinumab for pustular psoriasis are available because of the rarity of the disease.
Ayako Fujishige, Noriko Seko
wiley +1 more source
The emerging role of zinc transporters in cellular homeostasis and cancer [PDF]
, 2017 Zinc is an essential micronutrient that plays a role in the structural or enzymatic functions of many cellular proteins. Cellular zinc homeostasis involves the opposing action of two families of metal transporters: the ZnT (SLC30) family that functions ...
Bafaro, Elizabeth +3 more
core +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 5, Page 589-597, May 2025.Summary Background and Objectives: Generalized pustular psoriasis (GPP) is a rare, chronic, potentially life‐threatening skin disease. We aimed to establish criteria to accurately approximate GPP prevalence in Germany. Methods: A retrospective analysis of the WIG2 health claims database (1/1/2016–31/12/2020) was conducted.
Michael Schultze +4 more
wiley +1 more source
, 2005 J Pediatr Gastroenterol Nutr. 2005 Oct;41(4):483-4, 484. Clinical quiz. Prior AC, Selores M, Pina R, Dias JA, Costa FM, Vale L, Gomes L. Department of Pediatrics, Hospital Geral de Santo António, Portugal.
COSTA, F.M. +6 more
core +1 more source
Dermatologic Therapy, 2019 Acrodermatitis continua of Hallopeau (ACH) is a chronic, inflammatory, and relapsing disorder characterized by the progressive destruction of fingernails and toenails. This condition is rare, difficult to treat, and often misdiagnosed.
C. Lanna +7 more
semanticscholar +1 more source