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Research 571–600 of 1000+
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia.
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Molecular Genetics of Alopecias
- Focal and Generalized Alopecia
- The Effect of Simvastatin on Plasma Steroid Hormone Levels in Metformin-Treated Women with Non-Classic Congenital Adrenal Hyperplasia
- Disease causing homozygous variants in the human hairless gene
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Evaluation of Hair Loss
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS