Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Michael W Johnson"'
Autor:
Ramiro Castro Apolo, Preet Varade, Jaspreet Johal, Michael W Johnson, Adam Edwards Md, Michael R Persch, Hussam A. Yacoub
Publikováno v:
Hospital practice (1995). 50(3)
Introduction: Adult polyglucosan body disease (APBD) is an autosomal recessive leukodystrophy caused by abnormal intracellular accumulation of glycogen byproducts. This disorder is linked to a deficiency in glycogen branching enzyme-1 (GBE-1). Neurol
Autor:
Emil R. Unanue, Brian Saunders, Anthony N. Vomund, Javier A. Carrero, Bernd H. Zinselmeyer, Michael W. Johnson
Publikováno v:
Diabetologia
Aims/hypothesis We studied here the interactions between the resident macrophages of pancreatic islets with beta cells and the blood vasculature. We also examined the immunological consequences of such interactions. Methods Islets were isolated from
Autor:
Benjamin Pariente, Peter L. Wang, ILKe Nalbantoglu, Michael W. Johnson, Jean-François Rahier, Gwendalyn J. Randolph, Bernd H. Zinselmeyer, Jean-Frederic Colombel, Alex Kartheuser, Laurent Dubuquoy, Shashi Bala, Amélie Chau
Publikováno v:
The American Journal of Pathology. 186:3066-3073
Early pathological descriptions of Crohn disease (CD) argued for a potential defect in lymph transport; however, this concept has not been thoroughly investigated. In mice, poor healing in response to infection-induced tissue damage can cause hyperpe
Autor:
Stoyan Ivanov, Peter L. Wang, Ki-Wook Kim, Brian Saunders, Michael J. Davis, Jesse W. Williams, Emma L. Kuan, Brant E. Isakson, Gwendalyn J. Randolph, Bernd H. Zinselmeyer, Erica G. Weinstein, Carlos G. Briseño, Melissa Ouhachi, Reinhold Förster, Adam C. Straub, Joshua P. Scallan, Emmanuel L. Gautier, Michael W. Johnson, Marco Colonna, Kathrin Werth
Publikováno v:
Journal of Clinical Investigation
Journal of Clinical Investigation, 2016, 126 (4), pp.1581-1591. ⟨10.1172/JCI84518⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126, pp.1581-1591. ⟨10.1172/JCI84518⟩
Journal of Clinical Investigation, 2016, 126, pp.1581-1591. ⟨10.1172/JCI84518⟩
Journal of Clinical Investigation, 2016, 126 (4), pp.1581-1591. ⟨10.1172/JCI84518⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2016, 126, pp.1581-1591. ⟨10.1172/JCI84518⟩
Journal of Clinical Investigation, 2016, 126, pp.1581-1591. ⟨10.1172/JCI84518⟩
International audience; Lymphatic collecting vessels direct lymph into and from lymph nodes (LNs) and can become hyperpermeable as the result of a previous infection. Enhanced permeability has been implicated in compromised immunity due to reduced fl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89f274c1955c50e42524d6965a94126e
https://hal.science/hal-03798251
https://hal.science/hal-03798251
Autor:
Christine L. Hann, Gary L. Gallia, Alessandro Olivi, Avadhut D. Joshi, Michael W. Johnson, Gregory J. Riggins, Constance A. Griffin, Zev A. Binder
Publikováno v:
Clinical Neurology and Neurosurgery. 113:411-415
Muir–Torre syndrome (MTS) is an autosomal dominant subtype of nonpolyposis colorectal carcinoma (HNPCC) characterized by the development of sebaceous gland tumors and visceral malignancies. The most common subtype of MTS is characterized by germlin
Autor:
M.P.H. Lisa Stoll M.D., Olga Pletnikova, Michael W. Johnson, David R. Fowler, Juan Troncoso, Ana Rubio, Ling Li
Publikováno v:
Journal of Forensic Sciences. 56:1198-1205
We tested the independent utility of β-amyloid precursor protein (β-APP) immunohistochemical staining as evidence of brain trauma in the deaths of young children. Blinded reviewers retrospectively reviewed immunostained brain tissues from homicidal
Publikováno v:
Genetic Engineering & Biotechnology News. 36:32-33
Autor:
Arie Perry, Michael W. Johnson, Charles G. Eberhart, Tarik Tihan, Patricia T. Goldthwaite, Peter C. Burger, Soroush Rais-Bahrami, Kenneth J. Cohen, Marc K. Rosenblum
Publikováno v:
American Journal of Surgical Pathology. 34:1783-1791
To define the spectrum of pilomyxoid morphology and to characterize the association between pilomyxoid astrocytoma (PMA) and pilocytic astrocytoma (PA), 84 cases of pediatric astrocytomas with pilomyxoid features were reviewed. Forty-two of these tum
Publikováno v:
Diagnostic Cytopathology. 39:451-454
The vast majority of malignant pleural effusions are caused by metastatic adenocarcinoma, most frequently from breast or lung primaries. However, a minority of cases show evidence of involvement by a hematopoietic neoplasm such as lymphoma or leukemi
Publikováno v:
Diagnostic Cytopathology. 39:657-662
Papillary epithelial fragments (PEFs) are a rarely described architectural feature in cervicovaginal (Pap) smears. Morphologically, PEFs often consist of small, finely branching glandular tissue fragments with varying cytomorphology. This study ident