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Research 751–780 of 1000+
- 157 Analysis of the hybrid schwannoma and neurofibroma including a case report of schwannomatosis caused by a mutation in the LZTR1 gene
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC)
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 012 A Case Report of Central Centrifugal Cicatricial Alopecia in Two Generations
- A rare hair loss in children: Monilethrix
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Causes and Management of Hypertrichosis
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Generalized atrophic benign epidermolysis bullosa.
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Managing Cutaneous Manifestations of Hyperandrogenic Disorders
- Keratins: the hair shaft's backbone revealed
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Congenital atrichia associated with situs inversus and mesocardia
- Substance P in keratosis follicularis spinulosa decalvans
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Value of dermoscopy for the diagnosis of monilethrix
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Folliculin: A surprising molecular brake in the human hair follicle