Results 131 to 140 of about 6,674 (213)

Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss. [PDF]

Cureus
Moreno BA, Torres K, Duarte A.
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

A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights. [PDF]

BMC Med Genomics
Nejati P, Khosravi T, Lorestani S, Oladnabi M.   +3 more
europepmc   +1 more source

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

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

Christ Siemens Touraine syndrome: a case report [PDF]

, 2009
Luiz Gutenberg TM Coelho, Arnaldo F Caldas, Evelyne P Soriano, Veronica MS Rodrigues, Roseane S Costa, N Freire-Maia, J Zonana, U Mehta, C Drögemüller, J Kere, PH Itin, H van Bokhoven, TA Phan, AJ Hickey   +13 more
core   +1 more source

Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis. [PDF]

Australas J Dermatol
So N, Yip L, Orchard D.
europepmc   +1 more source

Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes [PDF]

, 2010
J Koochmeshgi, CC Li, L Petukhova, G Romeo, LP Kate Ten   +4 more
core   +1 more source

The First Colombian Patient with <i>CDH3</i>-Related Hypotrichosis with Juvenile Macular Dystrophy. [PDF]

Skin Appendage Disord
Prieto LE, Vasquez-Forero DM, Pachajoa H.   +2 more
europepmc   +1 more source