Results 61 to 70 of about 8,842 (142)

Preimplantation Genetic Diagnosis for DEB by Detecting a Novel Family-Specific COL7A1 Mutation in Vietnam

The Application of Clinical Genetics, 2021
Sang Trieutien,1,* Tam Vu Van,2,3,* My Tran Ngoc Thao,4 Son Trinh The,5 Khoa Tran Van,1 Tung Nguyen Thanh,5 Tuan Tran Van,5 Hanh Nguyen Thi6 1Department of Biology and Genetics, Vietnam Military Medical University, Hanoi, 12108, Vietnam ...
Trieutien S, Vu Van T, Tran Ngoc Thao M, Trinh The S, Tran Van K, Nguyen Thanh T, Tran Van T, Nguyen Thi H   +7 more
doaj  

Skin Fragility and Hyperpigmentation in a Patient With HIV

JEADV Clinical Practice, Volume 5, Issue 2, Page 716-718, June 2026.
Catalina Retamal, Maximiliano Maass, María Fernanda Martin   +2 more
wiley   +1 more source

Infant Spinal Anesthesia for Urologic Surgery in a Patient With Epidermolysis Bullosa

Case Reports in Anesthesiology
Infant spinal anesthesia presents a viable alternative to general anesthesia for short procedures below the umbilicus. This technique eliminates the need for airway instrumentation while preserving hemodynamic and respiratory parameters.
Alexander B. Froyshteter, Jillian A. Dibiase, Catherine M. Seager, Alina Lazar   +3 more
doaj   +1 more source

Bullae and Scales in a Newborn

JEADV Clinical Practice, Volume 5, Issue 2, Page 719-721, June 2026.
Hamad El Hajj, Dima Jeha, Andre Megarbane, Hala Megarbane   +3 more
wiley   +1 more source

Nail Dystrophy Treated With Marigold Therapy in a Patient With Epidermolysis Bullosa Simplex

Australasian Journal of Dermatology, Volume 67, Issue 4, Page e255-e256, June 2026.
Aalia Syed, M. Tariq Khan, Dédée F. Murrell   +2 more
wiley   +1 more source

EPIDERMOLYSIS BULLOSA HEREDITARIA: A DERMATOLOGIST‘S PERSPECTIVE AND NEWLY TREATMENT APPROACHES

Slovenska pediatrija
Epidermolysis bullosa is a genetically inherited disorder characterized by extreme skin fragility. Mutations in at least 20 different genes have been identified, leading to structural or functional abnormalities or the absence of proteins involved in the
Olga Točkova
doaj   +1 more source

The modern features of the clinics, diagnostics and treatment of patients with epidermolysis bullosa

Лечащий Врач, 2021
The article presents information on epidermolysis bullosa, a rare genetic skin disease caused by mutations of several genes responsible for the synthesis of structural proteins of the skin.
L. A. Yusupovа, E. I. Yunusovа, Z. Sh. Garaeva, G. I. Mavlyutova, M. A. Morozova   +4 more
doaj  

Wound nursing management of children with congenital epidermolysis bullosa

Huli yanjiu, 2016
It reviewed the research status quo of wound care of children with congenital epidermolysis bullosa(EB),based on epidermolysis bullosa“wound bed preparation”（WBP）from the wound management steps including the effective cleaning of the wound,the ...
任平, 陈劼, 张玉侠
doaj  

ISEV2026 Abstract Book

Journal of Extracellular Vesicles, Volume 15, Issue S1, June 2026.
wiley   +1 more source

Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature

BMC Pediatrics
Epidermolysis Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or near the dermal-epidermal junction are mutated recessively or dominantly, and this is the primary cause of EB.
Fatma Mabrouk Ali, Jieyu Zhou, Mingyan Wang, Qiuxia Wang, Lulu Sun, Mansour Maulid Mshenga, Hongyan Lu   +6 more
doaj   +1 more source