Results 71 to 80 of about 10,708 (219)
American Journal of Hematology, Volume 101, Issue 3, Page 467-476, March 2026.ABSTRACT Non‐severe aplastic anemia (NSAA) is a heterogeneous bone marrow failure syndrome with limited standardized treatment options. Cyclosporine A (CsA) monotherapy often yields suboptimal responses, highlighting an unmet clinical need for more effective therapies.
Lele Zhang +18 more
wiley +1 more source
Developmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source
Gingival fibromatosis with congenital hypertrichosis
Journal of Indian Society of Periodontology, 2020 Idiopathic gingival fibromatosis is a slowly progressive proliferative fibrous lesion of the gingival tissue, leading to functional, esthetic, and psychological difficulties.
Sameer Saxena +3 more
doaj +1 more source
Você Conhece Esta Síndrome? [PDF]
, 2013 POEMS syndrome is a unique clinical entity, the diagnosis of which is made when polyneuropathy and monoclonal gammopathy occur together, associated with other changes such as organomegaly, endocrinopathy, skin changes and papilledema.
João, A, Lestre, S, Santos, G
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Long‐Term Follow‐Up of Patients With Transaldolase Deficiency
Journal of Inherited Metabolic Disease, Volume 49, Issue 2, March 2026.ABSTRACT Transaldolase (TALDO) deficiency has a well‐characterized phenotype. However, there are few large cohort studies, and little is known about the long term, including the need for organ transplantation. Our aim was to share a long multicenter experience in managing these patients.
M. Scaglione +18 more
wiley +1 more source
Facial hair growth in a patient with psoriasis [PDF]
, 2016 info:eu-repo/semantics ...
Matos, R., Torres, T.
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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis [PDF]
, 2016 Twenty-six families with keratinopathic ichthyoses (epidermolytic ichthyosis, superficial epidermolytic ichthyosis or congenital reticular ichthyosiform erythroderma) were studied.
Betz, Regina C. +12 more
core +3 more sources
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 3, Page 372-381, March 2026.Summary Laser and energy‐based devices (EBDs) are firmly established in dermatology and widely used for both medical and aesthetic purposes. Even with advanced safety features such as integrated cooling and real‐time monitoring, these procedures still carry inherent risks.
Lynhda Nguyen +4 more
wiley +1 more source
Picturing another culture: Developing language proficiency, empathy, and visual literacy through art [PDF]
, 2019 Integrating art (paintings, sculptures, photography, and other types of images) into second language (L2) instruction, can have a positive effect on language acquisition and developing intercultural understanding.
Fegely, Kathy, Hoecherl-Alden, Gisela
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Equine Veterinary Education, Volume 38, Issue 3, Page e170-e179, March 2026.Summary Background Pituitary pars intermedia dysfunction (PPID) is commonly treated with pergolide mesylate, a dopamine receptor agonist. Cabergoline is a dopamine receptor agonist that has shown activity on prolactin secretion in horses for up to 10 days.
H. Hess +5 more
wiley +1 more source