Search
for
Sort by
Research 31–60 of 1000+
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Inherited Disorders of the Hair
- Hormonal acne: leading to a paradigm shift in the management of acne
- Alopecia in children
- Alopecia in Cronkhite-Canada syndrome
- Hair Follicle Miniaturization in a Woolly Hair Nevus
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Unruly hair
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- [Netherton's syndrome in two sisters].
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Dermatoscopy of hair shaft disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Cysteine and Glutamine level in hair shaft fractures patients
- Hair growth promoting effects of adipose tissue-derived stem cells
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Woolly hair nevus
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Hereditary, Congenital, and Acquired Alopecias
- Two females with hair loss
- Acquired progressive kinking of the hair in a prepubertal boy
- 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
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Diseases of the Hair and Nails
- Congenital hair loss disorders: Rare, but not too rare