Disorders of Hair and Nail
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-43630-2_7
Reference119 articles.
1. Kaler SG, Holmes CS, Goldstein DS, Tang J, Godwin SC, Donsante A, et al. Neonatal diagnosis and treatment of Menkes disease. N Engl J Med. 2008;358(6):605–14. doi: 10.1056/NEJMoa070613 .
2. Powell J, Dawber RP, Ferguson DJ, Griffiths WA. Netherton’s syndrome: increased likelihood of diagnosis by examining eyebrow hairs. Br J Dermatol. 1999;141(3):544–6.
3. Rakowska A, Kowalska-Oledzka E, Slowinska M, Rosinska D, Rudnicka L. Hair shaft videodermoscopy in netherton syndrome. Pediatr Dermatol. 2009;26(3):320–2. doi: 10.1111/j.1525-1470.2008.00778.x .
4. Korge BP, Hamm H, Jury CS, Traupe H, Irvine AD, Healy E, et al. Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype. J Invest Dermatol. 1999;113(4):607–12. doi: 10.1046/j.1523-1747.1999.00722.x .
5. Winter H, Vabres P, Larregue M, Rogers MA, Schweizer J. A novel missense mutation, A118E, in the helix initiation motif of the type II hair cortex keratin hHb6, causing monilethrix. Hum Hered. 2000;50(5):322–4. doi:22936.
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