Search
for
Sort by
Research 30 of 73
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Thallium poisoning: emphasis on early diagnosis and response to haemodialysis
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
- Woodhouse-Sakati syndrome (WSS)
- Cutaneous effects of the most commonly used antidepressant medication, the selective serotonin reuptake inhibitors
- Drugs that affect autonomic functions or the extrapyramidal system
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Pediatric Psychocutaneous Disorders
- Psychodermatology
- The IVIG treatment response in autoimmune polyendocrine syndromes type 2 with anti-GAD65 antibody-associated stiff person syndrome: a case report and literature review
- Arecaceae
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Targeting neurosteroid synthesis as a therapy for schizophrenia-related alterations induced by early psychosocial stress
- Reporting on Adverse Clinical Events
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- Psychotropic Medications and the Skin
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- A Case of Delusional Parasitosis Secondary to Severe Iron Deficiency Anaemia in a Tertiary Care Hospital: An Area for Clinical Vigilance
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Toxic and Metabolic Disorders of the Nervous System
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Selection of Anti-Depressants in Geriatric Dermatoses- A Questionnaire Study of Dermatologists in Western Rajasthan, India
- Adverse Cutaneous Reactions to Antipsychotics