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Research 511–540 of 1000+
- AN EDUCATIONAL PACKAGE ON LESSER KNOWN HERBAL MEDICINES IN INDIA
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Exploration of Therapeutic Ethno-Medicinal Plants used by Traditional Healers & Practitioners of Raichur District, Karnataka, India
- Extensive Challenges and Pending Advances in the Study of 5-Alpha-Reductase Isoenzymes. A Literature Review
- SYNTHETIC PIEZOELECTRIC POLYMERS AND THEIR APPLICATIONS IN MEDICINE; 2020-2021 OVERVIEW
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- 유전성 안드로겐탈모증의 임상적 고찰(제6보)
- Study on the distribution of hair keratin in normal hair follicles by immunohistochemical staining
- Chronic Alopecia
- 원저 : 안드로겐성 탈모증의 임상적 고찰
- Comorbid conditions associated with androgenic alopecia: A twin study
- Very-long-chain Acyl-CoA Synthetases
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Practical management of hair loss.
- Demographic Characteristics and Association of Serum Vitamin B12, Ferritin and Thyroid Function with Premature Canities in Indian Patients from an Urban Skin Clinic of North India: A Retrospective Analysis of 71 Cases.
- Dynamic Trichoscopy
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses