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Research 151–180 of 1000+
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Skin manifestations among<i>GATA2</i>-deficient patients
- Biotin Deficiency in a Patient with Short Bowel Syndrome during Home Parenteral Nutrition
- Cthrc1 deficiency aggravates wound healing and promotes cardiac rupture after myocardial infarction via non-canonical WNT5A signaling pathway
- Effect of Primary Biotin Deficiency on the Skin of Germ-Free and Conventional Mice Fed a Purified Biotin-Deficient Diet without Supplementation with Egg White.
- Studies on nutritional deficiency in cows in El-Behera province
- Deficiência de cobre condicionada a altos teores de zinco, manganês e ferro na região do Médio Paraíba, RJ, Brasil
- GSDMA deficiency impairs cutaneous squamous cell carcinoma growth
- Progressive Zinc and Iron Deficiency Following Bariatric Surgery in Iraqi Patients: A 12-Month Pilot Study
- Efficacy of Compound GV-350 with Tricofer® Iron, Cystine and Biotin in the Management of Telogen Effluvium in Women with Iron Deficiency
- Effect of iron-deficiency anemia on the outcomes of pregnancy, labor, and newborn health
- CHRONIC DIFFUSE TELOGENIC ALOPECIA IN FEMALE PERSONS AS A SIGN OF LATENT IRON DEFICIENCY (WITH CASE DESCRIPTION)
- Correction of Diffuse Alopecia in Iron Deficiency Anemia
- BH07: Testosterone deficiency in men with female pattern hair loss
- Network pharmacology and in vivo experimental analysis for validating the antifibrotic potential of Punica granatum leaves against skin scleroderma: the role of oxidative stress, inflammation and TGF-β1/Snail 1/p-Smad 3 signaling pathway
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- 5α-Metabolism in Finasteride-Treated Subjects and Male Pseudohermaphrodites with Inherited 5α-Reductase Deficiency
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- A study on common clinical pattern of presentation of skin and hair changes in nutritional deficiencies associated with dietary fallacies in children 1 to 5 years of age
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Vitamin D: A Bridging Element for Wellness; A Case Study on Vitamin D Deficiency and its Association with Alopecia Areata and Other Conditions
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Mixing the Old with the New: Drug Repurposing for Immune Deficiency in the Era of Precision Medicine and Pediatric Genomics
- The Role of Cytochrome P-450 in Dermatology
- 5-Alpha reductase deficiency
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates