Associated Papers
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion.
Schierz IAM et al.
Clinical Dysmorphology, 2020
Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndrome.
Piras R et al.
Human Mutation, 2014
Multiple small hyperintense lesions in the subcortical white matter on cranial MR images in two Turkish brothers with cold-induced sweating syndrome caused by a novel missense mutation in the CRLF1 gene.
Tüysüz B et al.
Brain & Development, 2013
Cold-induced sweating syndrome type 1, with a CRLF1 level mutation, previously associated with Crisponi syndrome.
González Fernández D et al.
Dermatology (basel, Switzerland), 2013
Cold-induced sweating syndrome: CISS1 and CISS2: manifestations from infancy to adulthood. Four new cases.
Hahn AF et al.
Journal of the Neurological Sciences, 2010
Cold-induced sweating syndrome with neonatal features of Crisponi syndrome: longitudinal observation of a patient homozygous for a CRLF1 mutation.
Yamazaki M et al.
American Journal of Medical Genetics. Part A, 2010
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