Results 141 to 150 of about 5,312 (215)

A Child with Hallermann-Streiff Syndrome; as an Infrequent Cause of Hypotrichosis and Cataract

, 2016
Sultan Kaba, Murat Doğan, Nesrin Ceylan, Keziban Bulan, Nihat Demir, Şekibe Zehra Doğan, Selami Kocaman   +6 more
openalex   +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

Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation(要約)

, 2016
美咲 木下
openalex   +1 more source

Light and scanning electron microscopic examination of late changes in hair with hereditary trichodysplasia (Marie Unna hypotrichosis)

, 2004
Hakan Hamdi Çelik, Hüseyin Sürücü, Mustafa M. Aldur, Bulent M. Ozdemir, Ayşen Karaduman, M Cumhur   +5 more
openalex   +2 more sources

Klinische und experimentelle Beobachtung über Alopecia (Hypotrichosis) congenita

, 1911
A. Büschke
openalex   +2 more sources

Hypotrichosis-deafness syndrome [PDF]

, 2020
openaire   +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

Hypotrichosis simplex of the scalp [PDF]

, 2020
openaire   +1 more source

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