Epidermolysis bullosa

A Bardhan, L Bruckner-Tuderman… - Nature reviews Disease …, 2020 - nature.com
Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses
characterized by mucocutaneous fragility and blister formation, inducible by often minimal …

Tfos dews ii pathophysiology report

AJ Bron, CS de Paiva, SK Chauhan, S Bonini… - The ocular …, 2017 - Elsevier
Abstract The TFOS DEWS II Pathophysiology Subcommittee reviewed the mechanisms
involved in the initiation and perpetuation of dry eye disease. Its central mechanism is …

Extracellular matrix reorganization during wound healing and its impact on abnormal scarring

M Xue, CJ Jackson - Advances in wound care, 2015 - liebertpub.com
Significance: When a cutaneous injury occurs, the wound heals via a dynamic series of
physiological events, including coagulation, granulation tissue formation, re …

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification

JD Fine, L Bruckner-Tuderman, RAJ Eady… - Journal of the American …, 2014 - Elsevier
Background Several new targeted genes and clinical subtypes have been identified since
publication in 2008 of the report of the last international consensus meeting on diagnosis …

[HTML][HTML] Amelogenesis imperfecta; genes, proteins, and pathways

CEL Smith, JA Poulter, A Antanaviciute… - Frontiers in …, 2017 - frontiersin.org
Amelogenesis imperfecta (AI) is the name given to a heterogeneous group of conditions
characterized by inherited developmental enamel defects. AI enamel is abnormally thin, soft …

Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009

V Oji, G Tadini, M Akiyama, CB Bardon… - Journal of the American …, 2010 - Elsevier
BACKGROUND: Inherited ichthyoses belong to a large, clinically and etiologically
heterogeneous group of mendelian disorders of cornification, typically involving the entire …

Диагностические индексы в дерматологии

ВП Адаскевич - 2014 - elibrary.ru
Книга посвящена систематизации количественной оценки дерматологических
заболеваний. Во второе издание вошли зарекомендовавшие себя на практике и …

Genome editing in induced pluripotent stem cells using CRISPR/Cas9

R Ben Jehuda, Y Shemer, O Binah - Stem Cell Reviews and Reports, 2018 - Springer
The development of the reprogramming technology led to generation of induced Pluripotent
Stem Cells (iPSC) from a variety of somatic cells. Ever since, fast growing knowledge of …

Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues

JD Fine, JE Mellerio - Journal of the American Academy of Dermatology, 2009 - Elsevier
Based upon case reports and small case series, it has been known for many years that
some types and subtypes of inherited epidermolysis bullosa (EB) may be at risk for …

[PDF][PDF] Федеральные клинические рекомендации по оказания медицинской помощи детям с Желчекаменной болезнью

АА Баранов… - МЗ РФ, Союз педиатров …, 2015 - vodb2.vologda.ru
2++ Высококачественные систематические обзоры исследований случай-контроль или
когортных исследований. Высококачественные обзоры исследований случай-контроль …