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Research 331–360 of 1000+
- Alopecia in Children: The Most Common Causes
- Focal and Generalized Alopecia
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Polycystic Ovary Syndrome (PCOS): From Diagnosis to Treatment
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review
- Clinical Management in Psychodermatology
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A new type of pachyonychia congenita.
- Building Models for Keratin Disorders
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Congenital hypotrichosis due to short anagen
- Advances in dermatology research: A comprehensive literature review
- Gender aspects in skin diseases
- Dermoscopy Research—An Update
- Cutaneous reactions to recombinant cytokine therapy
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The Function of Zinc in Animal, Plant, and Human Nutrition
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Low level of maternal biotin intake changes the expression of biotin transporter in dams and fetuses in mice
- Exploring Quality of Life Among Thyroid Patients in South Indian Communities: A Comprehensive Study
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Prevalence of Cutaneous Disorders in Patients with Polycystic Ovary Syndrome
- Genetic Defects of Female Sexual Differentiation
- Hair loss in children in South-East Nigeria: common and uncommon cases