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Research 211–240 of 1000+
- Woolly hair generalizado: caso clínico e revisão da literatura
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- A Retrospective Study of Frontal Fibrosing Alopecia from North-East India
- Congenital Atrichia: A Case Report
- Molecular Basis of Hereditary Hair Diseases
- Efficacy of an Oral Ageratum Conyzoides Formulation on Increasing Hair Growth and Decreasing Hair Loss in Males and Females: A Randomised Double-Blind Placebo-Controlled Study
- Frontal Fibrosing Alopecia: A prospective observational study
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Frontal fibrosing alopecia, clinical and histopathological characteristics of mexican patients: an original research study and review of literature
- Androgenetic Alopecia
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- UTILIZAÇÃO DE ISOTRETINOÍNA ORAL NO TRATAMENTO DA ALOPECIA FIBROSANTE FRONTAL: SÉRIE DE CASOS
- Clinical report of a Holstein's calf with ichthyosis.
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Frontal fibrosing alopecia: Histopathological and immunohistochemical study of the inflammatory infiltrate and the sebaceous gland receptors
- Cicatricial Alopecia with Particular Trichoscopic and Histopathological Features
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- 283 Thermal imaging and trichoscopy for detecting inflammation in frontal fibrosing alopecia
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- Frontal fibrosing alopecia: a pathology on the rise
- A generalized reticulate eruption with scarring alopecia, vulvovaginitis, keratoderma, and 20-nail dystrophy in a 70-year-old woman
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Woolly Hair in Two Siblings
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS