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Research 211–240 of 484
- Regulatory T Cells: the Many Faces of Foxp3
- Biology and Genetics of Hair
- 46,XY DSD due to impaired androgen production
- How to diagnose a lipodystrophy syndrome
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Dermatopathology and molecular genetics
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- A Newborn With Hair Loss
- The Role of Histone Demethylases in Disease
- Syndromes of Severe Insulin Resistance (SSIRs)
- Adrenal causes of endocrine hypertension in childhood or adolescence
- 5-Alpha reductase deficiency
- Diagnostic approach to low‐renin hypertension
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Bachmann–Bupp syndrome and treatment
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- FOXN1 deficient nude severe combined immunodeficiency
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Genetic Disorders and Defects in Vitamin D Action
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Myotonic Dystrophy—A Progeroid Disease?
- Pleiotropic Role of Notch Signaling in Human Skin Diseases