Woodhouse-Sakati Syndrome Latest Advances

Woodhouse-sakati syndrome with no reportable MRI findings: a case report.

Journal: BMC neurology

Published: February 07, 2024

Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant.

Journal: American journal of medical genetics. Part A

Published: June 08, 2023

Woodhouse-Sakati syndrome: A review.

Journal: Revue neurologique

Published: March 18, 2023

Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review.

Journal: Orphanet journal of rare diseases

Published: May 25, 2022

Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome.

Journal: Journal of neuroendocrinology

Published: October 06, 2021

Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene.

Journal: Frontiers in endocrinology

Published: September 05, 2021

Writer's Cramp Presentation of Woodhouse-Sakati Syndrome - "Out of the Woods".

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: August 24, 2021

Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies.

Journal: Saudi medical journal

Published: July 26, 2021

Expanding on the phenotypic spectrum of Woodhouse-Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review.

Journal: American journal of medical genetics. Part A

Published: June 24, 2021

Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.

Journal: Journal of clinical laboratory analysis

Published: June 11, 2021

Quantitative Susceptibility Mapping in Woodhouse-Sakati Syndrome.

Journal: Annals of neurology

Published: April 02, 2021

Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome.

Journal: Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society

Published: January 08, 2021

Woodhouse-Sakati Syndrome Latest Advances

Find the Latest Research About Woodhouse-Sakati Syndrome

Woodhouse-sakati syndrome with no reportable MRI findings: a case report.

Woodhouse-sakati syndrome with no reportable MRI findings: a case report.

Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant.

Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant.

Woodhouse-Sakati syndrome: A review.

Woodhouse-Sakati syndrome: A review.

Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review.

Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review.

Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome.

Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome.

Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene.

Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene.

Writer's Cramp Presentation of Woodhouse-Sakati Syndrome - "Out of the Woods".

Writer's Cramp Presentation of Woodhouse-Sakati Syndrome - "Out of the Woods".

Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies.

Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies.

Expanding on the phenotypic spectrum of Woodhouse-Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review.

Expanding on the phenotypic spectrum of Woodhouse-Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review.

Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.

Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family.

Quantitative Susceptibility Mapping in Woodhouse-Sakati Syndrome.

Quantitative Susceptibility Mapping in Woodhouse-Sakati Syndrome.

Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome.

Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome.