Results 141 to 150 of about 14,748 (240)

An infant of KID syndrome along with Dandy-Walker malformation (DWM). [PDF]

JAAD Case Rep
Mondal A.
europepmc   +1 more source

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

A case report of palmoplantar keratoderma in a 3-year-old girl: A structured approach in primary care settings. [PDF]

Malays Fam Physician
Mohd Noor AA, Abdul Hadi A, Che Abdul Rahim AR.   +2 more
europepmc   +1 more source

Patch-Type Granuloma Annulare [PDF]

, 2009
Afonso, A, Cardoso, J, Carvalho, R, Coelho, R, Rodrigues, A   +4 more
core   +1 more source

How skin achieves mechano-resistance for land movement: the critical role of ER sensing. [PDF]

Cell Regen
Fu W, Li H, Ning W.
europepmc   +1 more source

Kindler Syndrome in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report. [PDF]

Case Rep Dermatol Med
Ahmad DS, Nasser R, Mahmoud A, Al-Janabi MH, Al-Shehabi Z, Hassan F.   +5 more
europepmc   +1 more source

Association of hidradenitis suppurativa disease severity with increased risk for systemic comorbidities [PDF]

, 2015
Crowley, JJ, Gu, Y, Kerdel, F, Kimball, A, Mekkes, JR, Okun, MM, Scheinfeld, N, Sundaram, M, Zouboulis, CC   +8 more
core   +1 more source

Successful treatment of an <i>MBTPS2</i>-linked Olmsted syndrome patient using erlotinib. [PDF]

JAAD Case Rep
Sadeghzadeh-Bazargan A, Khodakarim N, Liafuii MN, Zeinali R, Safaei A, Youssefian L, Dehghani A, Vahidnezhad H.   +7 more
europepmc   +1 more source

Huriez Syndrome. [PDF]

Indian Dermatol Online J
Singh S, Das S.
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