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Research 481–510 of 1000+
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Rare Association of Congenital Triangular Alopecia with Vitiligo
- Clinical and Trichoscopic Characteristics in a Case of Congenital Triangular Alopecia
- Hypotrichosis in a child with olmsted syndrome
- Oral Presentations
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- 6 Current concepts of polycystic ovary syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Prevalence of metabolic syndrome in the family members of women with polycystic ovary syndrome from North India
- Metabolic syndrome – a new definition and management guidelines A joint position paper by the Polish Society of Hypertension, Polish Society for the Treatment of Obesity, Polish Lipid Association, Polish Association for Study of Liver, Polish Society of Family Medicine, Polish Society of Lifestyle Medicine, Division of Prevention and Epidemiology Polish Cardiac Society, “Club 30” Polish Cardiac Society, and Division of Metabolic and Bariatric Surgery Society of Polish Surgeons
- Female Adolescent Hair Disorders
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Plasma levels of C19 steroid glucuronides in pre-menopausal women with non-classical congenital adrenal hyperplasia
- Congenital atrichia with papular lesions
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Influence of Vitamin D on the Incidence of Metabolic Syndrome and Hormonal Balance in Patients with Polycystic Ovary Syndrome
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- A clinico-social study of polycystic ovarian syndrome in women of reproductive age group at tertiary care centre
- The Potential Utility of Tirzepatide for the Management of Polycystic Ovary Syndrome
- Female Pelvic Conditions: Polycystic Ovary Syndrome.
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- A case of unilateral congenital triangular alopecia
- Approaches to lifestyle management in polycystic ovary syndrome
- Clinical interest of a nonchemical lotion in head lice management
- Early-onset Male Androgenetic Alopecia and Metabolic Syndrome: Are They Associated?
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle