Results 41 to 50 of about 675 (153)
Современные аспекты лечения витилиго [PDF]
, 2022 ВИТИЛИГО /ДИАГН /ТЕРПАТОГЕНЕЗТОПИЧЕСКАЯ ТЕРАПИЯСВЕТОЛЕЧЕНИЕ /ИСПФОТОРАДИАЦИОННАЯ ТЕРАПИЯ /ИСПФОТОТЕРАПИЯ /ИСПВитилиго является приобретенным гипомеланозом с частотой встречаемости 0,1%-2% среди взрослого и детского населения во всем мире.
Катина, М. А.
core +1 more source
Erythropoietic Protoporphyria: You May Not Have Seen It, but It May Have Seen You [PDF]
, 2022 Erythropoietic protoporphyria is a rare skin condition that commonly presents in childhood. We report a case of a 35-year-old Hispanic male with a history of sun sensitivity, presenting with complaints of immediate burning and itching of the skin on his ...
Hsu, Sylvia +3 more
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Rare disease prevention and treatment:The need for a level playing field [PDF]
, 2018 Pharmacogenetic tests are being used increasingly to prevent rare and potentially life-threatening adverse drug reactions. For many tests, however, cost–effectiveness is hard to demonstrate, and with the exception of a few cases, widespread ...
Hughes, Dyfrig, Plumpton, Catrin
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MC1R FUNCTIONS, EXPRESSION, AND IMPLICATIONS FOR TARGETED THERAPY [PDF]
, 2021 The G protein-coupled MC1R is expressed in melanocytes and has a pivotal role in human skin pigmentation, with reduced function in human genetic variants exhibiting a red hair phenotype and increased melanoma predisposition.
Colin Goding +2 more
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Medicine Access @ Point of Care, 2019 Patient representation during the evaluation of medicines by key decision makers such as regulatory agencies, Health Technology Assessment bodies, and healthcare payers is increasingly considered to add value to the appraisals and empowers patients ...
Jasmin Barman-Aksözen
doaj +1 more source
Cutaneous Porphyrias:Causes, symptoms, treatments and the Danish incidence 1989-2013 [PDF]
, 2016 Porphyrias are rare diseases caused by altered haem synthesis leading to the accumulation of different haem intermediates. Neurovisceral attacks may occur in acute porphyrias, while photosensitivity is the presenting symptom in cutaneous porphyrias.
Aagaard, Lise +4 more
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Важливість молекулярно-генетичних досліджень при гіпохромній мікроцитарній анемії, рефрактерній до феротерапії, у діагностиці еритропоетичної протопорфірії [PDF]
, 2022 Еритропоетична протопорфірія (ЕПП) є рідкісним спадковим захворюванням, зареєстрованим в усьому світі, проте існують регіональні відмінності у його епідеміології.
A.M. Mykh +5 more
core +2 more sources
Cytoprotection Concepts for Ischemic Stroke in the Recanalization Era
Advanced Science, Volume 13, Issue 18, 27 March 2026.This review provides detailed information on modern cytoprotective strategies for ischemic stroke in the context of recanalization therapies. It derives their rationale based on contemporary knowledge of stroke pathophysiology and discusses the role of advanced imaging approaches as well as concepts for novel clinical trial designs.
Johannes Boltze, Marc Fisher
wiley +1 more source
Melanocortin receptors in GtoPdb v.2023.1 [PDF]
, 2023 Melanocortin receptors (provisional nomenclature as recommended by NC-IUPHAR [41]) are activated by members of the melanocortin family (α-MSH, β-MSH and γ-MSH forms; δ form is not found in mammals) and adrenocorticotrophin (ACTH ...
Caruso, Vanni +14 more
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ChemistrySelect, Volume 11, Issue 6, 12 February 2026.The Seplife Fmoc‐RinkAmide‐PS‐PEG resin, a PEG‐grafted PS resin with optimized composition enables improved swelling and higher loading for SPPS. This resin delivers efficient couplings and high crude purities, supporting reliable synthesis of long and complex peptides.
Ashish Kumar +12 more
wiley +1 more source