Sofia Babay
Jerusalem, JM, Israel
Last Updated: 09/26/2026
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Found 8 publications
H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.
Journal: Acta dermato-venereologica
Published: May 28, 2015
Two Novel Homozygous Desmoplakin Mutations in Carvajal Syndrome.
Journal: Pediatric dermatology
Published: April 01, 2015
Generalized verrucosis and HPV-3 susceptibility associated with CD4 T-cell lymphopenia caused by inherited human interleukin-7 deficiency.
Journal: Journal of the American Academy of Dermatology
Published: December 01, 2014
IL36RN mutation causing generalized pustular psoriasis in a Palestinian patient.
Journal: International journal of dermatology
Published: June 06, 2014
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair.
Journal: Journal of medical genetics
Published: March 28, 2014
Ophthalmologic Findings in H Syndrome: A Unique Diagnostic Clue.
Journal: Ophthalmic genetics
Published: February 20, 2014
H syndrome: the first 79 patients.
Journal: Journal of the American Academy of Dermatology
Published: June 05, 2013
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.
Journal: Arthritis and rheumatism
Published: September 29, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026