M. Schwartz

发表

Best treatment practices for pachyonychia congenita

E. Sprecher, I. Goldberg, D. Fruchter, 2014, Journal of the European Academy of Dermatology and Venereology : JEADV.

The molecular genetic analysis of the expanding pachyonychia congenita case collection

E. Sprecher, W. McLean, E. O’Toole, 2013, The British journal of dermatology.

The molecular genetic analysis of the expanding pachyonychia congenita case

E. Sprecher, W. McLean, E. O’Toole, 2014 .

Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16

F. Smith, K. Spaunhurst, K. Zeman, 2012, The British journal of dermatology.

Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children

E. Sprecher, E. Warshauer, F. Smith, 2019, The British journal of dermatology.

Comparative Study of High-Resolution Multifrequency Ultrasound of the Plantar Skin in Patients with Various Types of Hereditary Palmoplantar Keratoderma

E. Sprecher, D. Gaitini, I. Goldberg, 2013, Dermatology.

Mutations in GJB6 causing phenotype resembling pachyonychia congenita

N. Wilson, M. Zamiri, F. Smith, 2015, British Journal of Dermatology.

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

C. Cole, A. Irvine, M. McAleer, 2017, The British journal of dermatology.

A large mutational study in pachyonychia congenita.

S. Leachman, W. McLean, P. Hull, 2011, The Journal of investigative dermatology.

Recessive mutations in the gene encoding frizzled 6 cause twenty nail dystrophy--expanding the differential diagnosis for pachyonychia congenita.

W. McLean, C. Kocabaş, P. Hull, 2013, Journal of dermatological science (Amsterdam).

A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita.

S. Leachman, Mark J. Eliason, C. Hansen, 2012, Journal of the American Academy of Dermatology.