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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

La myasthénie et sa délimitation

Warter, Jean Marie. January 1971 (has links)
Thesis--Strasbourg. / "No 118." Includes bibliographical references (leaves [i]-xxv).
2

Immunopathogenesis and nasal tolerance in experimental autoimmune myasthenia gravis /

Shi, Fu-Dong, January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 9 uppsatser.
3

La myasthénie et sa délimitation

Warter, Jean Marie. January 1971 (has links)
Thesis--Strasbourg. / "No 118." Includes bibliographical references (leaves [i]-xxv).
4

Studies on the epidemiology of myasthenia gravis in Finland and its clinical and neuro-physiological aspects

Hokkanen, Eero. January 1969 (has links)
Academic diss.--Helsinki. / Includes bibliographical references.
5

Murine T and B cell epitodes within the human recombinant acetylcholine receptor alpha-subunit

Palace, Jacqueline Ann January 1991 (has links)
No description available.
6

The induction of tolerance in CD4+ lymphocytes in vitro using soluble MHC class II : peptide complexes; a model for specific immunotherapy in autoimmune disease

Nicolle, Michael W. January 1994 (has links)
No description available.
7

Studies of immune mechanisms in myasthenia gravis /

Xu, Biying, January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 5 uppsatser.
8

Cardiopulmonary rehabilitation for a patient with myasthenia gravis

Farrell, Jennifer A. January 1900 (has links) (PDF)
Thesis (D.PT.)--Sage Colleges, 2009. / "May 2009." "A Capstone project for PTY 768 presented to the Faculty of the Department of Physical Therapy Sage Graduate School in partial fulfillment of the requirements for the degree of Doctor of Physical Therapy." Includes bibliographical references.
9

Age-related resistance to experimental autoimmune myasthenia gravis immunological and neurobiological aspects /

Hoedemaekers, Cornelia Wilhelmina Elisabeth. January 1997 (has links)
Proefschrift Universiteit Maastricht. / Auteursnaam op omslag: Astrid Hoedemaekers. Met bibliogr., lit. opg. - Met samenvatting in het Nederlands.
10

Miastenia gravis no Ceará, Brasil : aspectos clínicos e epidemiológicos

Aguiar, Aline de Almeida Xavier January 2010 (has links)
AGUIAR, Aline de Almeida Xavier. Miastenia gravis no Ceará, Brasil : aspectos clínicos e epidemiológicos. 2010. 117 f. Dissertação (Mestrado em Ciêcias Médicas) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2010. / Submitted by denise santos (denise.santos@ufc.br) on 2013-01-18T16:05:21Z No. of bitstreams: 1 2010_dis_aaxaguiar.pdf: 755701 bytes, checksum: 53d91cb84d6291d111a641e9804b6b8b (MD5) / Approved for entry into archive by Erika Fernandes(erikaleitefernandes@gmail.com) on 2013-01-23T11:45:14Z (GMT) No. of bitstreams: 1 2010_dis_aaxaguiar.pdf: 755701 bytes, checksum: 53d91cb84d6291d111a641e9804b6b8b (MD5) / Made available in DSpace on 2013-01-23T11:45:14Z (GMT). No. of bitstreams: 1 2010_dis_aaxaguiar.pdf: 755701 bytes, checksum: 53d91cb84d6291d111a641e9804b6b8b (MD5) Previous issue date: 2010 / A retrospective chart review of patients diagnosed as having myasthenia gravis, followed in Hospital Universitário Walter Cantídio, Hospital Geral de Fortaleza and by neurologists in Ceará, Brazil, from October 1981 to June 2009 was performed. Clinical and epidemiologic aspects were evaluated. In this work, 122 patients were studied, of whom 85 (69.7%) were females and 37 (30.3%) were males. The disease duration ranged from five months to 50 years (8.9 ± 8.1 years). Age at the first symptoms varied from 0 to 74 years (31.9 ± 14.4 years). The main first symptoms and signs were ptosis, diplopia and member weakness. Generalized myasthenia was the most common clinical presentation, but 5.1% (n=6) persisted as ocular myasthenia. Thymectomy was performed in 42.6% (n=52) of myasthenic patients. A thymoma was present in 10 patients. Serum acetylcholine receptor (AChR) antibodies were present in 80% (n=20) of specimens tested. / Foram analisados, retrospectivamente, os prontuários de pacientes com diagnóstico de miastenia grave (MG), diagnosticados e seguidos no Hospital Universitário Walter Cantídio, Hospital Geral de Fortaleza e por neurologistas que tratavam doenças neuromusculares, no período de outubro de 1981 a junho de 2009 no Estado do Ceará, Brasil. Foram coletados dados clínicos e epidemiológicos. Foram estudados 122 pacientes, sendo 85 (69.7%) do sexo feminino e 37 (30.3%) do sexo masculino. O tempo de duração da doença variou de cinco meses a 50 anos (8.9 ± 8.1 anos). A idade de inicio da doença variou de zero a 74 anos (31.9 ± 14.4 anos). Na amostra estudada, os primeiros sintomas foram principalmente ptose palpebral superior, diplopia e fraqueza dos membros. A maioria dos pacientes apresentou a forma generalizada, enquanto 5.1% (n= 6) persistiram com miastenia ocular. Timectomia foi realizada em 42.6% (n=52) dos pacientes. A presença de timoma foi demonstrada em 10 pacientes. Anticorpos anti-receptor de acetilcolina estavam presentes em 80% (n=20) das amostras testadas.

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