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Research 61–90 of 1000+
- Keratosis follicularis spinulosa decalvans in a family
- Treatment of monilethrix with oral minoxidil
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- <i>De novo</i> mutations in monilethrix
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Hair That Is Difficult to Manage in a Hispanic Girl
- <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
- Assessment of scalp hair survivin in patients with premature greying of hair
- Office Diagnosis of Hair Shaft Defects
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Loose anagen syndrome in one identical twin girl.
- Clouston’s Syndrome-A Case Report
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Short anagen hair syndrome
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Polycystic ovarian disease in adult and perimenopausal women