Amanote Research

Amanote Research

    RegisterSign In

Challenges of the Differential Diagnosis Between the Subtypes of the Junctional Epidermolysis Bullosa: Presentation of Two Clinical Cases

Almanac of Clinical Medicine
doi 10.18786/2072-0505-2019-47-009
Full Text
Open PDF
Abstract

Available in full text

Date

February 26, 2019

Authors
Yu. Yu. KotalevskayaN. M. Marycheva
Publisher

Moscow Regional Research and Clinical Institute (MONIKI)


Related search

Junctional Epidermolysis Bullosa

2020English

Prenatal Diagnosis of Junctional Epidermolysis Bullosa Associated With Pyloric Atresia.

Journal of Medical Genetics
Genetics
1990English

Epidermolysis Bullosa - A Report of Two Cases

Annals of Dentistry
2002English

Junctional Epidermolysis Bullosa, Generalized Intermediate

2020English

Laminin 332 in Junctional Epidermolysis Bullosa

Cell Adhesion and Migration
Molecular NeuroscienceCell BiologyCellular
2013English

414 Uncovering the Cause of Early Lethality in Generalized Severe Junctional Epidermolysis Bullosa

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2019English

Digenic Junctional Epidermolysis Bullosa: Mutations in COL17A1 and LAMB3 Genes

American Journal of Human Genetics
Genetics
1999English

Junctional Epidermolysis Bullosa: Allelic Heterogeneity and Mutation Stratification for Precision Medicine

Frontiers in Medicine
Medicine
2019English

A Silent COL17A1 Variant Alters Splicing and Causes Junctional Epidermolysis Bullosa

Acta Dermato-Venereologica
DermatologyMedicine
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy