Search
for
Sort by
Research 421–450 of 1000+
- Nutrition and Hair
- Towards a molecular understanding of hair loss and its treatment
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- The Effect of 5 -Reductase Inhibitors on Erectile Function
- Friends Turned Foes: Angiogenic Growth Factors beyond Angiogenesis
- Evolving approaches to profiling the microbiome in skin disease
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hair Shaft Dysplasias
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Clinical Approach to the Patient With Alopecia
- Evaluation and Management of the Hair Loss Patient in the Primary Care Setting
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- National scientific medical meeting 1996 abstracts
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy