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Research 151–180 of 1000+
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Exploring obesity-related endocrine disorders beyond diabetes: a narrative review
- The Prevalence of Polycystic Ovary Syndrome, Its Phenotypes and Cardio-Metabolic Features in a Community Sample of Iranian Population: Tehran Lipid and Glucose Study
- An Indian Evidence-Based Study of Prevalence, Phenotypic Features, Lifestyle Modifications of Polycystic Ovarian Syndrome Patients
- Androgen excess disorders remain undiagnosed in one of every four premenopausal women with Type 1 diabetes
- Detection of the nuclear translocation of androgen receptor using quantitative and automatic cell imaging analysis
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Dermatomyositis Disease in Dogs
- 773 Generation of human hair follicle organoids in vitro and ex vivo by co-culture of primary human hair matrix keratinocytes and dermal papilla fibroblasts
- The Clinical Presentation of Systemic Lupus Erythematosus
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- The diagnosis and treatment of iron deficiency and its potential relationship to hair loss
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- COLLAB: A Global Survey of Clinical and Laboratory Assessment in Alopecia Areata by Hair Specialists
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Alopecia Areata: Updates from the Mouse Perspective
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Study on Autoimmune Thyroid Disorders in Chronic Spontaneous Urticaria at a Tertiary Care Central Rural Hospital in India
- An Update of Congenital Adrenal Hyperplasia
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Identification of Drug-Disease Associations Using Information of Molecular Structures and Clinical Symptoms via Deep Convolutional Neural Network
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Caring for women with polycystic ovary syndrome