Results 141 to 150 of about 8,285 (255)

Epidermal barrier disorders and corneodesmosome defects [PDF]

, 2014
Marek Haftek
core   +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

Correction: Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report. [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

Congenital Hypotrichosis in a Child [PDF]

Proceedings of the Royal Society of Medicine, 1933
openaire   +2 more sources

Topical minoxidil effectiveness in enhancing facial aesthetics: A systematic review and meta-analysis. [PDF]

J Family Med Prim Care
Almutairi AG, Shadid A, AlAkrash L.
europepmc   +1 more source

Keratoderma-hypotrichosis-leukonychia Totalis Syndrome: A New Case Report of an Exceptional Entity. [PDF]

Acta Derm Venereol
Gutiérrez-Cerrajero C, Gestoso-Uzal N, Ortiz-Cabrera NV, González-Sarmiento R, Hernández-Martín Á.   +4 more
europepmc   +1 more source

Hypotrichosis-deafness syndrome [PDF]

, 2020
openaire   +1 more source

Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review. [PDF]

Clin Exp Pediatr
Ghosh U, Agrawal A, Srinivasan VM, Manisha R, Shukla U, Jain V, Nilay M, Kumar H.   +7 more
europepmc   +1 more source

Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex.

American Journal of Human Genetics, 2018
M. Romano, A. Tafazzoli, M. Mattern, S. Sivalingam, S. Wolf, A. Rupp, H. Thiele, J. Altmüller, P. Nürnberg, J. Ellwanger, R. Gambon, A. Baumer, N. Kohlschmidt, D. Metze, S. Holdenrieder, R. Paus, D. Lütjohann, J. Frank, M. Geyer, M. Bertolini, P. Kokordelis, R. Betz   +21 more
semanticscholar   +1 more source

Dental and Craniofacial Findings in Early Childhood in Oral-Facial-Digital Syndrome Type 1: A Case Report. [PDF]

Case Rep Dent
Saygili S, Kasimoglu Y.
europepmc   +1 more source