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Research 781–810 of 1000+
- Association between Alopecia Areata, Psoriasis Vulgaris, Thyroid Disease, and Metabolic Syndrome
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Post-Finasteride Syndrome: An Induced Delusional Disorder with the Potential of a Mass Psychogenic Illness?
- Cantú syndrome with coexisting familial pituitary adenoma
- Co-presentation of Tapia's syndrome and pressure alopecia—A rare event after septorhinoplasty: A case report and literature review
- Female pattern hair loss: beyond an androgenic aetiology?
- Tufted hair folliculitis in a patient affected by pachydermoperiostosis: case report and videodermoscopic features.
- A Case of Satoyoshi Syndrome: A Multisystem Disorder
- A rare case of woolly hair with unusual associations
- Alopecia areata with white hair regrowth: case report and review of poliosis
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Successful induction of oral tolerance in Netherton syndrome
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Adult-onset Satoyoshi syndrome in a young male
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Cushing's syndrome due to pharmacological interaction in a cystic fibrosis patient
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Refractory dermatomyositis–systemic lupus erythematosus overlap syndrome and response to tofacitinib
- Cutaneous manifestations of polycystic ovary syndrome
- Association Between Premature Hair Greying and Metabolic Risk Factors: A Cross-sectional Study
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- What Syndrome Is This?
- SARS-CoV-2 vaccination complicated by small fiber neuropathy, mast cell activation syndrome, and pericarditis
- Finasteride for hair loss: a review