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- Three siblings with Woodhouse-Sakati syndrome in an Indian family.
Woodhouse-Sakati syndrome consists of alopecia, hypogonadism, diabetes mellitus, mild mental retardation, sensorineural deafness and ECG... - Dystonia in the Woodhouse Sakati syndrome: A new family and...
Woodhouse Sakati syndrome is a rare autosomal recessive neuroendocrine disorder characterized by the combination of alopecia, hypogonadism, diabetes - Studies from Christian Medical College, Department of Endocrinology...
A report, 'Three siblings with Woodhouse-Sakati syndrome in an Indian family,' is newly published data in Clinical Dysmorphology (see also Life - Woodhouse-Sakati syndrome: case report and symptoms review.
We report on a 52-year old Caucasian woman exhibiting signs of Woodhouse - Sakati syndrome and review the clinical signs and symptoms in patients - Role of cofactors B (TBCB) and E (TBCE) in tubulin heterodimer...
Understanding the in vivo function of these proteins will shed light on the Kenny-Caffey/Sanjad-Sakati syndrome, an important human disorder... - Four siblings with distal renal tubular acidosis and...
Faqeih, E; Al-Akash, SI; Sakati, N; et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A 143A (17): 1951-1957 SEP 1 2007... - Articles parus en septembre 2007
Résumé ... 45. Faqeih E, Al-Akash SI, Sakati N, Teebi PA. Four siblings with distal renal tubular acidosis and nephrocalcinosis, neurobehavioral...