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Research 601–630 of 1000+
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Polycystic ovary syndrome
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- Recent Approaches in the Treatment of Polycystic Ovary Syndrome: An Update
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Netherton Syndrome – Responding to Oral Retinoids
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Trichothiodystrophy: Current Concepts
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Alopecia totalis in an infant
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Hirsutism causes and treatments.
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- A Clinical Review of Trichorrhexis Nodosa
- Keratins and skin disease
- Lithium toxicity profi le: a systematic review and meta-analysis
- Effect of Oral Minoxidil on Monilethrix
- Trichoscopic Evaluation of Focal Non-Cicatricial Alopecia in Egyptian Children
- Pili torti in association with citrullinemia
- Complex X chromosome rearrangement associated with multiorgan autoimmunity