-
1
-
-
85027925412
-
The molecular genetic analysis of the expanding pachyonychia congenita case collection
-
Wilson NJ, O'Toole E, Milstone LM, et al,. The molecular genetic analysis of the expanding pachyonychia congenita case collection. Br J Dermatol 2014; 171: 343-55.
-
(2014)
Br J Dermatol
, vol.171
, pp. 343-355
-
-
Wilson, N.J.1
O'Toole, E.2
Milstone, L.M.3
-
2
-
-
84865397810
-
A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita
-
Eliason MJ, Leachman SA, Feng BJ, et al,. A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita. J Am Acad Dermatol 2012; 67: 680-6.
-
(2012)
J Am Acad Dermatol
, vol.67
, pp. 680-686
-
-
Eliason, M.J.1
Leachman, S.A.2
Feng, B.J.3
-
4
-
-
79954570064
-
The phenotypic and molecular genetic features of pachyonychia congenita
-
McLean WH, Hansen CD, Eliason MJ, Smith FJ,. The phenotypic and molecular genetic features of pachyonychia congenita. J Invest Dermatol 2011; 131: 1015-17.
-
(2011)
J Invest Dermatol
, vol.131
, pp. 1015-1017
-
-
McLean, W.H.1
Hansen, C.D.2
Eliason, M.J.3
Smith, F.J.4
-
5
-
-
76349084709
-
First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder
-
Leachman SA, Hickerson RP, Schwartz ME, et al,. First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder. Mol Ther 2010; 18: 442-6.
-
(2010)
Mol Ther
, vol.18
, pp. 442-446
-
-
Leachman, S.A.1
Hickerson, R.P.2
Schwartz, M.E.3
-
6
-
-
70349987628
-
Rapamycin selectively inhibits expression of an inducible keratin (K6a) in human keratinocytes and improves symptoms in pachyonychia congenita patients
-
Hickerson RP, Leake D, Pho LN, et al,. Rapamycin selectively inhibits expression of an inducible keratin (K6a) in human keratinocytes and improves symptoms in pachyonychia congenita patients. J Dermatol Sci 2009; 56: 82-8.
-
(2009)
J Dermatol Sci
, vol.56
, pp. 82-88
-
-
Hickerson, R.P.1
Leake, D.2
Pho, L.N.3
-
8
-
-
38149039350
-
Mice expressing a mutant Krt75 (K6hf) allele develop hair and nail defects resembling pachyonychia congenita
-
Chen J, Jaeger K, Den Z, et al,. Mice expressing a mutant Krt75 (K6hf) allele develop hair and nail defects resembling pachyonychia congenita. J Invest Dermatol 2008; 128: 270-9.
-
(2008)
J Invest Dermatol
, vol.128
, pp. 270-279
-
-
Chen, J.1
Jaeger, K.2
Den, Z.3
-
10
-
-
84871261443
-
Eccrine sweat glands are major contributors to reepithelialization of human wounds
-
Rittié L, Sachs DL, Orringer JS, et al,. Eccrine sweat glands are major contributors to reepithelialization of human wounds. Am J Pathol 2013; 182: 163-71.
-
(2013)
Am J Pathol
, vol.182
, pp. 163-171
-
-
Rittié, L.1
Sachs, D.L.2
Orringer, J.S.3
-
11
-
-
84884225406
-
Comparative study of high-resolution multifrequency ultrasound of the plantar skin in patients with various types of hereditary palmoplantar keratoderma
-
Goldberg I, Sprecher E, Schwartz ME, Gaitini D,. Comparative study of high-resolution multifrequency ultrasound of the plantar skin in patients with various types of hereditary palmoplantar keratoderma. Dermatology 2013; 226: 365-70.
-
(2013)
Dermatology
, vol.226
, pp. 365-370
-
-
Goldberg, I.1
Sprecher, E.2
Schwartz, M.E.3
Gaitini, D.4
-
13
-
-
84155170863
-
v1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker
-
v1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker. Pain 2012; 153: 80-5.
-
(2012)
Pain
, vol.153
, pp. 80-85
-
-
Goldberg, Y.P.1
Price, N.2
Namdari, R.3
-
14
-
-
84885019283
-
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting
-
Samuelov L, Sarig O, Harmon RM, et al,. Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting. Nat Genet 2013; 45: 1244-8.
-
(2013)
Nat Genet
, vol.45
, pp. 1244-1248
-
-
Samuelov, L.1
Sarig, O.2
Harmon, R.M.3
-
15
-
-
84863251177
-
Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome
-
Lin Z, Chen Q, Lee M, et al,. Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome. Am J Hum Genet 2012; 90: 558-64.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 558-564
-
-
Lin, Z.1
Chen, Q.2
Lee, M.3
-
16
-
-
84873426374
-
APR-246/PRIMA-1(MET) rescues epidermal differentiation in skin keratinocytes derived from EEC syndrome patients with p63 mutations
-
Shen J, van den Bogaard EH, Kouwenhoven EN, et al,. APR-246/PRIMA-1(MET) rescues epidermal differentiation in skin keratinocytes derived from EEC syndrome patients with p63 mutations. Proc Natl Acad Sci U S A 2013; 110: 2157-62.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 2157-2162
-
-
Shen, J.1
Van Den Bogaard, E.H.2
Kouwenhoven, E.N.3
-
17
-
-
79960847839
-
Pachyonychia congenita with laryngeal obstruction
-
Haber RM, Drummond D,. Pachyonychia congenita with laryngeal obstruction. Pediatr Dermatol 2011; 28: 429-32.
-
(2011)
Pediatr Dermatol
, vol.28
, pp. 429-432
-
-
Haber, R.M.1
Drummond, D.2
-
18
-
-
84882775674
-
The development of chronic pain: Physiological CHANGE necessitates a multidisciplinary approach to treatment
-
Pergolizzi J, Ahlbeck K, Aldington D, et al,. The development of chronic pain: physiological CHANGE necessitates a multidisciplinary approach to treatment. Curr Med Res Opin 2013; 29: 1127-35.
-
(2013)
Curr Med Res Opin
, vol.29
, pp. 1127-1135
-
-
Pergolizzi, J.1
Ahlbeck, K.2
Aldington, D.3
-
19
-
-
80052610907
-
Topical capsaicin for pain management: Therapeutic potential and mechanisms of action of the new high-concentration capsaicin 8% patch
-
Anand P, Bley K,. Topical capsaicin for pain management: therapeutic potential and mechanisms of action of the new high-concentration capsaicin 8% patch. Br J Anaesth 2011; 107: 490-502.
-
(2011)
Br J Anaesth
, vol.107
, pp. 490-502
-
-
Anand, P.1
Bley, K.2
|