Search
for
Sort by
Research 61–90 of 1000+
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Familial congenital generalized hypertrichosis
- Trichothiodystrophy in a child with occult learning disorder
- Anti‐Fertility Effects of Amlodipine in Adult Male Wistar Rats
- Developmental and reproductive outcome of F1 generation of Wistar rats exposed to Acanthus montanus aqueous extract during organogenesis
- Alopecia Areata with Renal Dysgenesis
- A 9-month-old infant with severe scalp dermatosis
- Emotional Consequences of Finasteride: Fool’s Gold
- HairSentinel: a time-aware anomaly detection framework for forecasting hairfall trends using temporal fusion transformers
- Is there male androgenetic alopecia the sign of male equivalent of polycystic ovary syndrome or metabolic syndrome
- Hormonale Diagnostik der sogenannten androgenetischen Alopezie der Frau
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Combination of Netherton Syndrome and Hypopituitarism with Isolated Somatotropin Deficiency: Case Study
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2)
- Contents
- Pigmentary mosaicism: An update
- Study of the Thyroid Profile of Patients with Alopecia
- Abstracts from the 2009 Annual Meeting of the Society for Pediatric Dermatology
- Cloning and Activity of Mouse Ultra-High Sulfur Keratin Gene Promoter