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Research 31–60 of 70
- How to diagnose a lipodystrophy syndrome
- Psychodermatology
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Pediatric Psychocutaneous Disorders
- Cluster Headache-Acute and Prophylactic Therapy
- Blockbuster Weight-Loss Drugs Not Tied to Suicidality, Studies Show
- Hypersensitivity to intravenous ondansetron: a case report
- Trichotillomania: What Do We Know So Far?
- Quality of life in Romanian patients with schizophrenia based on gender, type of schizophrenia, therapeutic approach, and family history
- A Case of Delusional Parasitosis Secondary to Severe Iron Deficiency Anaemia in a Tertiary Care Hospital: An Area for Clinical Vigilance
- “Doctor, You Must Examine My Creature Collection!”: A Case Report of Delusional Infestation
- Selection of Anti-Depressants in Geriatric Dermatoses- A Questionnaire Study of Dermatologists in Western Rajasthan, India
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Thallium poisoning: emphasis on early diagnosis and response to haemodialysis
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- 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”
- Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
- Woodhouse-Sakati syndrome (WSS)
- 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 Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Psychocutaneous disease
- Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and<i>UBTF</i>Genes
- The IVIG treatment response in autoimmune polyendocrine syndromes type 2 with anti-GAD65 antibody-associated stiff person syndrome: a case report and literature review
- Swastyayanam of Bhela indriya Sthana - an explorative study
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family