Zobrazeno 1 - 10
of 11
pro vyhledávání: '"M G, Heckman"'
Autor:
E. A. Waller, J. F. Aduen, D. J. Kramer, F. Alvarez, M. G. Heckman, J. E. Crook, O. E. Pajaro, L. R. McBride, C. A. Keller
Publikováno v:
Mayo Clinic Proceedings. 82:1502-1508
Publikováno v:
Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus. 28(1)
Nutcracker esophagus (NE) is a common esophageal motility disorder chacterized by high amplitude peristaltic contractions in the distal esophagus. While previous studies have examined selected aspects of this condition (e.g. pathogenesis and treatmen
Publikováno v:
Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus. 25(3)
Diffuse esophageal spasm (DES) remains insufficiently understood. Here we aimed to summarize the demographic, clinical, radiographic, and manometric features in a large cohort of patients with DES. We identified all consecutive patients diagnosed wit
Autor:
J C, Dachsel, C, Wider, C, Vilariño-Güell, J O, Aasly, A, Rajput, A H, Rajput, T, Lynch, D, Craig, A, Krygowska-Wajs, B, Jasinska-Myga, G, Opala, M, Barcikowska, K, Czyzewski, R-M, Wu, M G, Heckman, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 18(8)
Mutations of the LRRK2 gene are now recognized as major risk factors for Parkinson's disease. The Lrrk2 protein is a member of the ROCO family, which also includes Lrrk1 and Dapk1. Functional genetic variants of the DAPK1 gene (rs4877365 and rs487810
Publikováno v:
Alimentary pharmacologytherapeutics. 33(11)
Eosinophilic oesophagitis clinically presents with recurrent episodes of dysphagia and food impaction. Recently, we observed patients with noncardiac chest pain and eosinophilic oesophagitis.To estimate the prevalence of abnormal eosinophilic infiltr
Autor:
C, Wider, C, Vilariño-Güell, M G, Heckman, B, Jasinska-Myga, A I, Ortolaza-Soto, N N, Diehl, J E, Crook, S A, Cobb, J A, Bacon, J O, Aasly, J M, Gibson, T, Lynch, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 18(6)
Recent evidence suggests that variation in the SNCA, MAPT, and GSK3B genes interacts in affecting risk for Parkinson disease (PD). In the current study, we attempt to validate previously published findings, evaluating gene-gene interactions between S
Autor:
C, Wider, C, Vilariño-Güell, B, Jasinska-Myga, M G, Heckman, A I, Soto-Ortolaza, S A, Cobb, J O, Aasly, J M, Gibson, T, Lynch, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 17(3)
Whilst an association between the tau gene (MAPT)-containing H1 haplotype and supranuclear gaze palsy (PSP) has long been recognized, the effect of H1 on risk for Parkinson's disease (PD) has remained more contentious.Herein, we examined the associat
Autor:
A I, Soto-Ortolaza, B, Behrouz, C, Wider, C, Vilariño-Güell, M G, Heckman, J O, Aasly, J, Mark Gibson, T, Lynch, B, Jasinska-Myga, A, Krygowska-Wajs, G, Opala, M, Barcikowska, K, Czyzewski, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 17(2)
Calcium levels have been proposed to play an important role in the selective vulnerability of nigrostriatal dopaminergic neurons in Parkinson's disease (PD). Recently, an association was reported between the calcium buffer, calbindin (rs1805874) and
Publikováno v:
The Quarterly journal of medicine. 55(218)
The lymphoproliferative disorders and the myelodysplastic syndromes are thought to result from the clonal expansion of a single abnormal precursor cell. Seven patients who were found to have concurrent myelodysplasia and lymphoproliferation are descr
Autor:
S H, Tsung, M G, Heckman
Publikováno v:
Archives of pathology. 98(5)