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Research 121–150 of 1000+
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Dermatomyositis Disease in Dogs
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Androgenic alopecia and differential diagnoses of alopecia
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Loose anagen syndrome in one identical twin girl.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Delayed Puberty
- Acne-Associated Syndromes
- Polycystic ovarian disease in adult and perimenopausal women
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Biology and Genetics of Hair
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Monilethrix
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome