These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
81 related articles for article (PubMed ID: 23553204)
21. Reflectance confocal microscopy for the diagnosis of Galli-Galli disease. Coelho de Sousa V; El-Shabrawi-Caelen L; Mendes-Bastos P; Oliveira A Int J Dermatol; 2017 Dec; 56(12):1501-1504. PubMed ID: 28703363 [No Abstract] [Full Text] [Related]
22. Glucocerebrosidase N370S and L444P mutations as risk factors for Parkinson's disease in Brazilian patients. Guimarães Bde C; Pereira AC; Rodrigues Fda C; dos Santos AV; Campos M; dos Santos JM; dos Santos FL; de Rosso AL; Nicaretta DH; Pereira JS; da Silva DJ; Della Coletta MV; Santos-Rebouças CB; Pimentel MM Parkinsonism Relat Disord; 2012 Jun; 18(5):688-9. PubMed ID: 22192918 [No Abstract] [Full Text] [Related]
23. Changing a concept--controversy on the confusing spectrum of the reticulate pigmented disorders of the skin. Müller CS; Pföhler C; Tilgen W J Cutan Pathol; 2009 Jan; 36(1):44-8. PubMed ID: 18564280 [TBL] [Abstract][Full Text] [Related]
24. [Transient acantholytic dermatosis (Grover)]. Korom I; Földes M; Tóth-Kása I Z Hautkr; 1984 Jun; 59(11):750, 755-8. PubMed ID: 6485448 [TBL] [Abstract][Full Text] [Related]
25. Early histopathologic changes in grover disease. Melwani PM; Parsons AC; Sangueza OP Am J Dermatopathol; 2010 Aug; 32(6):565-7. PubMed ID: 20520528 [TBL] [Abstract][Full Text] [Related]
26. Screening for POLG W748S and A467T mutations in ataxia patients from Spain. Pelayo-Negro AL; Sánchez-Quintana C; Rodríguez-Oroz MC; Volpini V; Zeviani M; Tola-Arribas MA; Berciano J; Infante J Mov Disord; 2012 Sep; 27(10):1326. PubMed ID: 22711370 [No Abstract] [Full Text] [Related]
27. A novel mutation (p.Thr198Ser) in the 1A helix of keratin 5 causes the localized variant of epidermolysis bullosa simplex. Bowden PE; Knight AG; Liovic M Exp Dermatol; 2009 Jul; 18(7):650-2. PubMed ID: 19220453 [TBL] [Abstract][Full Text] [Related]
28. Large-scale case-control study of a functional polymorphism in the glutamate receptor, metabotropic 3 gene in patients with schizophrenia. Nunokawa A; Watanabe Y; Kitamura H; Kaneko N; Arinami T; Ujike H; Inada T; Iwata N; Kunugi H; Itokawa M; Ozaki N; Someya T Psychiatry Clin Neurosci; 2008 Apr; 62(2):239-40. PubMed ID: 18412850 [No Abstract] [Full Text] [Related]
30. Association between the SLC6A12 gene and negative symptoms of schizophrenia in a Korean population. Park HJ; Kim JW; Lee SK; Kim SK; Park JK; Cho AR; Chung JH; Song JY Psychiatry Res; 2011 Oct; 189(3):478-9. PubMed ID: 21367462 [TBL] [Abstract][Full Text] [Related]
31. Novel keratin 5 mutations in epidermolysis bullosa simplex: cases with unusual genotype-phenotype correlation. Oh SW; Lee JS; Kim MY; Kim SC J Dermatol Sci; 2007 Dec; 48(3):229-32. PubMed ID: 17855059 [No Abstract] [Full Text] [Related]
39. Ultrastructure of acantholysis in pemphigus foliaceus re-examined from the current perspective. van der Wier G; Jonkman MF; Pas HH; Diercks GF Br J Dermatol; 2012 Dec; 167(6):1265-71. PubMed ID: 22835262 [TBL] [Abstract][Full Text] [Related]
40. [The spectrum of transient acantholytic dermatoses]. Lang I; Lindmaier A; Hönigsmann H Hautarzt; 1986 Sep; 37(9):485-93. PubMed ID: 3771215 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]