Results 131 to 140 of about 5,635 (205)

Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis. [PDF]

Front Med (Lausanne)
Xie Y, Luo S, Yang Y, Zou X, Lv S, Du M, Xu Y, Song X, Qi C, Li N, Yang D.   +10 more
europepmc   +1 more source

Desmosomal-Type Acantholysis-A New Histologic Pattern Related to Mutations of Genes for Desmosomal Proteins. [PDF]

Dermatopathology (Basel)
Metze D, Süßmuth K, Metze C, Oji V, Traupe H.   +4 more
europepmc   +1 more source

Clinical Spectrum and Genetic Variability in Ectodermal Dysplasia-Skin Fragility Syndrome. [PDF]

Indian Dermatol Online J
Gupta M, Sharma A, Chatterjee D, Vinay K.   +3 more
europepmc   +1 more source

A classical variant of ectodermal dysplasia: a case report. [PDF]

Pan Afr Med J
Jawade S, Wankhede P, Sharma R, Munjewar P, More V.   +4 more
europepmc   +1 more source

The first report of hypohidrotic ectodermal dysplasia caused by a novel mutation and accompanied with pathological femoral neck fracture: A case report. [PDF]

Medicine (Baltimore)
Liang GH, Meng XN, Juma T, Cao YP, Zhang DJ.   +4 more
europepmc   +1 more source

Importance of Different Parameters for Monitoring Dogs with <i>Leishmania infantum</i> Infections in a Non-Endemic Country. [PDF]

Pathogens
Kaempfle M, Dorsch R, Zablotski Y, Hartmann K, Bergmann M.   +4 more
europepmc   +1 more source

Clinical Presentation of a Family Diagnosed With Marie Unna Hereditary Hypotrichosis 1 Caused by a Novel Variant in HRURF. [PDF]

Pediatr Dermatol
Holm SØ, Graversen L, Simonsen AKW, Blechingberg J, Herlin LK, Rønholt K.   +5 more
europepmc   +1 more source

Hypohidrotic ectodermal dysplasia syndrome in a Sudanese patient: a case report. [PDF]

Pan Afr Med J
Mukhtar MA, Amine AAA, Muctar SA, Ibrahim ME, Mohamed HS.   +4 more
europepmc   +1 more source

Hypotrichosis-deafness syndrome [PDF]

, 2020
openaire   +1 more source

Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report. [PDF]

Dermatol Reports
Alwunais K, Alqahtani J, Aljalfan A, Alotaibi H.   +3 more
europepmc   +1 more source