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Research 541–570 of 1000+
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- 4 Vitamin D resistance
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- A Newborn With Hair Loss
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- The character “hairless” in the mouse
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Woolly hair generalizado: caso clínico e revisão da literatura
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- 302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa
- Werner′s syndrome
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Biotinidase deficiency characterized by skin and hair findings
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Disease causing homozygous variants in the human hairless gene