• A new case of Menkes syndrome. Prenatal exclusion diagnosis in a subsequent pregnancy
• A patient with onychotrichodysplasia, neutropenia and normal intelligence
• Acquired trichorrhexis nodosa: how to diagnose it?
• Alopecia in genetic diseases
• Bazex-Dupré-Christol syndrome. Follicular atrophoderma, multiple basal cell carcinomas and hypotrichosis
• Bazex, Dupré and Christol syndrome. Apropos of a case with prolymphocytic leukemia
• Breaking the cycle of hair breakage: pearls for the management of acquired trichorrhexis nodosa
• Characterization of tiger-tail banding and hair shaft abnormalities in trichothiodystrophy
• Chronic diarrhea and skin hyperpigmentation: a new association
• Clinical and laboratory features of the Menkes disease
• Corrigendum: Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome
• Cuticle cell defects in lamellar ichthyosis hair and anomalous hair shaft syndromes visualized after detergent extraction
• Dermatologic findings of focal dermal hypoplasia (Goltz syndrome)
• Development of cancer (vulvar cancer) in the Netherton syndrome (ichthyosis, hair anomalies, atopic diathesis)
• Ectodermal abnormalities in patients with Kabuki syndrome
• Ethnic hair disorders
• Evaluation of hair structural abnormalities in children with different neurological diseases
• Further evidence for autosomal dominant inheritance and ectodermal abnormalities in Kabuki syndrome
• Hair loss in children
• Hair Loss: Common Causes and Treatment
• Hair-shaft abnormality in a 7-year-old girl. Trichorrhexis nodosa dueto biotinidase deficiency
• Hereditary hypotrichosis simplex of the scalp
• Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: a new genetic syndrome?
• Ichthyosis vulgaris, growth retardation, hair dysplasia, tooth abnormalities, immunologic deficiencies, psychomotor retardation and resorption disorders. Case report of 2 siblings
• Identifying Mutations of the Tetratricopeptide Repeat Domain 37 (TTC37) Gene in Infants With Intractable Diarrhea and a Comparison of Asian and Non-Asian Phenotype and Genotype: A Global Case-report Study of a Well-Defined Syndrome With Immunodeficiency
• Intractable diarrhea of infancy with facial dysmorphism, trichorrhexis nodosa, and cirrhosis
• Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder
• Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency
• Keratoderma, hypotrichosis and leukonychia totalis: a new syndrome?
• Lanceolate hair-J (lahJ): a mouse model for human hair disorders
• Laron syndrome (primary growth hormone insensitivity): a unique model to explore the effect of insulin-like growth factor 1 deficiency on human hair
• Light microscopic hair abnormalities in children: retrospective review of 119 cases in a 10-year period
• Menkes disease--an autopsy case with metal analysis of hair
• Menkes' kinky hair disease: report of 2 cases
• Menkes' syndrome (trichopoliodystrophy): use of scanning electron-microscope in diagnosis and carrier identification
• Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)
• Netherton syndrome
• Netherton's syndrome: a severe neonatal disease. A case report
• Neurocutaneous syndrome with hair alterations
• Neurotrichosis: hair-shaft abnormalities associated with neurological diseases
• Noonan syndrome with loose anagen hair associated with trichorrhexis nodosa and trichoptilosis
• Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome
• Painful callosities in a young boy
• Pathogenesis in trichorrhexis invaginata (bamboo hair)
• Structural hair shaft abnormalities in hypomelanosis of ito and other ectodermal dysplasias
• Syndromic (phenotypic) diarrhea in early infancy
• The Arid Melancholy-Netherton Syndrome With Protein Energy Malnutrition
• The Netherton syndrome: clinical characteristics, differential diagnosis and new ways of therapy
• Tricho-Hepato-Eenteric Syndrome: Same Genotype but Different Phenotypes in Two Pakistani Children
• Tricho-hepato-enteric syndrome presenting with mild colitis
• Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report
• Trichorrhexis nodosa after hair transplantation: dermoscopic, pathologic and electron microscopy analyses
• Trichorrhexis nodosa and lip pits in autosomal dominant ectodermal dysplasia--central nervous system malformation syndrome
• Trichorrhexis nodosa due to repetitive trivial trauma
• Trichorrhexis nodosa: a distinctive presentation after tumour necrosis factor-α inhibitor therapy
• Trichoscopy in Hair Shaft Disorders
• Wooly hair syndrome. Clinical and microscopic study