Results 281 to 290 of about 9,324,018 (299)

Deficiency of the Tangier Disease Gene Abca1 Is Associated With Microglial Defects in Mice

International Journal of Developmental Neuroscience
Microglia, the resident macrophages of the central nervous system, are a diverse population that develop during embryonic and postnatal stages in the mouse.
Tomas Celis, Oriana Ramírez-Herrera, Myrna Barraza, Susan Calfunao, F. Saavedra, Patricia Romo-Toledo, Dolores Busso, Nicolas Santander   +7 more
semanticscholar   +1 more source

A case report of Tangier disease presents with acute sensorimotor polyneuropathy and its treatment approach.

Journal of Clinical Lipidology, 2023
Saniye Karabudak, Vildan Güzel, Beril Güler, Bulent Uyanik, Azize Esra Gürsoy   +4 more
semanticscholar   +1 more source

Sensory-motor not length-dependent multineuropathy followed by the syringomyelia-like phenotype: a novel presentation of Tangier disease

Neurological Sciences, 2022
Eleonora Sabatelli, M. Luigetti, Umberto Costantini, Gabriele Lucioli, A. Conte   +4 more
semanticscholar   +1 more source

Unusual diagnosis of Tangier disease during screening colonoscopy

Zeitschrift für Gastroenterologie - German Journal of Gastroenterology, 2022
G. Semmler, H. Hofer, R. Huber, W. März, F. Ofner, B. Wernly, C. Datz   +6 more
semanticscholar   +1 more source

Investigating the role of Miglustat in the management of a patient with Tangier Disease

http://isrctn.com/, 2021
T. Hiwot, A. Cook
semanticscholar   +1 more source

A case of mesenteric panniculitis in a patient with Tangier disease.

Journal of Clinical Lipidology, 2021
A. Townson, Yogeshkumar Malam, Katy Surman, Shaan Chhabra, C. Y. Tan, P. Deegan, J. Mathews   +6 more
semanticscholar   +1 more source

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Nature Genetics, 1999
A. Brooks-Wilson, M. Marcil, S. M. Clee, Lin-hua Zhang, K. Roomp, Marjel J van Dam, Lu Yu, C. Brewer, J. Collins, H. Molhuizen, O. Loubser, B.F. Francis Ouelette, K. Fichter, K. J. Ashbourne-Excoffon, C. Sensen, S. Scherer, Stephanie Mott, M. Denis, D. Martindale, J. Frohlich, K. Morgan, B. Koop, S. Pimstone, J. Kastelein, J. Genest, M. Hayden   +25 more
semanticscholar   +1 more source

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

Nature Genetics, 1999
M. Bodzioch, E. Orso, J. Klucken, T. Langmann, A. Böttcher, Wendy Diederich, W. Drobnik, S. Barlage, C. Büchler, M. Porsch-Özçürümez, W. Kaminski, H. Hahmann, K. Oette, G. Rothe, C. Aslanidis, K. Lackner, G. Schmitz   +16 more
semanticscholar   +1 more source

Is Tangier disease a rare cause of premature ovarian insufficiency?: A case report.

Journal of Clinical Lipidology
A. Babayeva, E. Cerit, G. Kayhan, Arda Inan, M. Akturk   +4 more
semanticscholar   +1 more source

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

Nature Genetics, 1999
S. Rust, Marie Rosier, H. Funke, J. Real, Z. Amoura, J. Piette, J. Deleuze, H. Brewer, N. Duverger, P. Denéfle, G. Assmann   +10 more
semanticscholar   +1 more source