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Research 601–630 of 1000+
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair.
- A University Center for the Performing Arts
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Current Genetics in Hair Diseases
- A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Keratosis follicularis spinulosa decalvans in a family
- Nonclassic 21-hydroxylase deficiency
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Treatment of monilethrix with oral minoxidil
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Pili Annulati: A case series and proposal for classification
- Moniletherix
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- Netherton Syndrome Associated with Growth Hormone Deficiency