Search
for
Sort by
Research 301–330 of 1000+
- Dermoscopy: A rapid bedside tool to assess monilethrix
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Synaptic processes and immune-related pathways implicated in Tourette syndrome
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Skin Pigmentation Types, Causes and Treatment—A Review
- Myotonic Dystrophy—A Progeroid Disease?
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- Integrative insights into polycystic ovarian syndrome (PCOS): A comparative review of unani and modern medical perspective
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- A brief report on PCOS: and its inducing model
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Vitamin D and skin diseases: A review
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- 5-Alpha reductase deficiency
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Roles of the Hedgehog Signaling Pathway in Cutaneous Physiology and Oncology
- Zinc and Zinc Transporters in Dermatology
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL