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Bibliografie tematiche / Syringomyelia Immunology

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Letteratura scientifica selezionata sul tema "Syringomyelia Immunology"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 6 febbraio 2022

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Articoli di riviste sul tema "Syringomyelia Immunology"

1

Yanık, Burcu, Safiye Tuncer, and Bülent Seçkin. "Neuropathic arthropathy caused by Arnold–Chiari malformation with syringomyelia." Rheumatology International 24, no. 4 (November 26, 2003): 238–41. http://dx.doi.org/10.1007/s00296-003-0389-x.

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2

Lu, Feng, Zan Chen, Hao Wu, and Feng-Zeng Jian. "Magnetic Resonance Imaging of Chiari Malformation Type I in Adult Patients with Dysphagia." BioMed Research International 2019 (May 14, 2019): 1–6. http://dx.doi.org/10.1155/2019/7485010.

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Abstract (sommario):

Objective. To explore the magnetic resonance imaging (MRI) characteristics of Chiari malformation type I (CMI) in patients with dysphagia. Methods. Adult patients diagnosed with CMI were retrospectively and consecutively reviewed from January 2013 to December 2016. Symptoms and medical characteristics were recorded. According to the clinical manifestations, we divided the patients into two groups. The first group had 21 patients with symptoms of dysphagia and the second group had 71 patients with nondysphagia symptoms. Various length or angle measurements of the posterior cranial fossa (PCF),

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3

Nacir, Baris, S. Arslan Cebeci, E. Cetinkaya, A. Karagoz, and H. R. Erdem. "Neuropathic arthropathy progressing with multiple joint involvement in the upper extremity due to syringomyelia and type I Arnold-Chiari malformation." Rheumatology International 30, no. 7 (June 23, 2009): 979–83. http://dx.doi.org/10.1007/s00296-009-1013-5.

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4

Shen, Jian, Jie Shen, Kaiyuan Huang, Yixin Wu, Jianwei Pan, and Renya Zhan. "Syringobulbia in Patients with Chiari Malformation Type I: A Systematic Review." BioMed Research International 2019 (March 19, 2019): 1–8. http://dx.doi.org/10.1155/2019/4829102.

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Abstract (sommario):

This study aimed to summarize the clinical features, diagnosis, and treatment of Chiari malformation type I- (CM-1-) associated syringobulbia. We performed a literature review of CM-1-associated syringobulbia in PubMed, Ovid MEDLINE, and Web of Science databases. Our concerns were the clinical features, radiologic presentations, treatment therapies, and prognoses of CM-1-associated syringobulbia. This review identified 23 articles with 53 cases. Symptoms included headache, neck pain, cranial nerve palsy, limb weakness/dysesthesia, Horner syndrome, ataxia, and respiratory disorders. The most fr

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5

Reece, Donna E., Giovanni Piza Rodriguez, Andrew Belch, David Szwajcer, Michael J. Kovacs, Chaim Shustik, Nizar J. Bahlis, et al. "Prospective Canadian Trial In Newly Diagnosed Multiple Myeloma Patients with t(4;14): Bortezomib-Based Therapy without ASCT." Blood 116, no. 21 (November 19, 2010): 1968. http://dx.doi.org/10.1182/blood.v116.21.1968.1968.

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Abstract (sommario):

Abstract Abstract 1968 Two previous studies have reported that multiple myeloma (MM) patients (pts) with t(4;14), identified by FISH cytogenetics, experience a median progression-free survival (PFS) of only 8–9 mos and median overall survival (OS) of 18 mos when treated with a single ASCT (Chang H, et al. Bone Marrow Transplant 2005; 36: 793; Gertz M, et al. Blood 2005; 106: 2837). On the other hand, the novel agent bortezomib is efficacious in relapsed myeloma pts with t(4;14). Based on these observations, we designed a phase II protocol for newly diagnosed MM pts with t(4;14) that consists o

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6

Berio, Agostino, Giacomo Garlaschi, Giuseppe Mangiante, Gian Luigi Mariottini, and Attilia Piazzi. "Chiari I malformation, syringomyelia and papilledema: a malformative complex connected to oculo-auriculo-vertebral spectrum." Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale 92, no. 1 (March 8, 2019). http://dx.doi.org/10.4081/jbr.2019.8001.

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Abstract (sommario):

The authors discuss the association of papilledema with Chiari I malformation (CMI) and syringomyelia on the basis of a clinical case studied by radiology, immunology and biochemistry methods. In the presence of normal haematology, blood immunology and biochemistry, clinical signs of headache and papilledema associated to hemifacial asymmetry, blind neck fistulas, malformed ears and spinal abnormalities (symptoms of oculo-auricolo- vertebral spectrum - OAVS), were observed. Magnetic resonance images and computed tomography demonstrated the occurrence of lowered cerebellar tonsils, but with val

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Tesi sul tema "Syringomyelia Immunology"

1

Lee, Gabriel Y. F. (Gabriel Yin Foo). "Origin of macrophages in rat syringomyelia : an investigative study using rat radiation bone marrow chimeras." 2001. http://web4.library.adelaide.edu.au/theses/09MS/09msl478.pdf.

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