Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Jani-Acsadi A"'
Autor:
Jani-Acsadi, Agnes, Lisak, Robert P.
Publikováno v:
In Journal of the Neurological Sciences 2007 261(1):127-133
Publikováno v:
Journal of Pediatric Neurology. :311-319
This paper reviews the spectrum of vasculitides that affect the brain, specifically focusing on primary angiitis of the central nervous system (CNS) and how they relate to stroke in the pediatric population. CNS vasculitis accounts for a substantial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8bc9efdd917ef0d9886a3ec529189a7
https://doi.org/10.3233/jpn-2010-0400
https://doi.org/10.3233/jpn-2010-0400
Autor:
Agnes Jani-Acsadi, Richard A. Lewis
Publikováno v:
Neuromuscular Disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a9047102aa0ecca43ed3a05b8170a49
https://doi.org/10.1002/9781119973331.ch25
https://doi.org/10.1002/9781119973331.ch25
Autor:
Agnes, Jani-Acsadi, Robert P, Lisak
Publikováno v:
Current Treatment Options in Neurology. 12:231-243
Treatment of patients with acquired (autoimmune) myasthenia gravis should rely on evidence-based therapeutic choices, taking into account the individual's needs according to disease severity (mild to severe), extent (ocular or generalized), comorbidi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbd8e79c540b134ba04afba903eaad1d
https://doi.org/10.1007/s11940-010-0070-0
https://doi.org/10.1007/s11940-010-0070-0
Publikováno v:
Pediatric clinics of North America. 62(3)
Heritable diseases of the peripheral nerves (Charcot-Marie-Tooth disease [CMT]) affect the motor units and sensory nerves, and they are among the most prevalent genetic conditions in the pediatric patient population. The typical clinical presentation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2345ebe77ae2c7296e13d23e0d0767c
https://pubmed.ncbi.nlm.nih.gov/26022174
https://pubmed.ncbi.nlm.nih.gov/26022174
Autor:
Agnes, Jani-Acsadi, Richard A, Lewis
Publikováno v:
Handbook of clinical neurology. 115
Demyelinating neuropathies are typically characterized by physiological slowing of conduction velocity and pathologically by segmental loss of myelin and in some instances, evidence of remyelination. Clinically, patients with demyelinating neuropathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e4e93bb262f164d79d8a776d7a231a9
https://pubmed.ncbi.nlm.nih.gov/23931785
https://pubmed.ncbi.nlm.nih.gov/23931785
Autor:
Agnes Jani-Acsadi, Richard A. Lewis
Demyelinating neuropathies are typically characterized by physiological slowing of conduction velocity and pathologically by segmental loss of myelin and in some instances, evidence of remyelination. Clinically, patients with demyelinating neuropathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::015b79bd4e1bf4a8fc0ed1a26f6041b3
https://doi.org/10.1016/b978-0-444-52902-2.00015-1
https://doi.org/10.1016/b978-0-444-52902-2.00015-1
Autor:
Peggy Allred, Robert H. Baloh, Duanduan Ma, Agnes Jani-Acsadi, Alan Pestronk, Shaughn Bell, Mariacristina Scoto, Matthew B. Harms, E.P. Tuck, Richard B. Vallee, Lindsey J. Miller, Mary M. Reilly, M. Al-Lozi, Francesco Muntoni, Kassandra M. Ori-McKenney, Michael E. Shy, S. Masi
Publikováno v:
Neurology. 78(22)
Objective: To identify the gene responsible for 14q32-linked dominant spinal muscular atrophy with lower extremity predominance (SMA-LED, OMIM 158600). Methods: Target exon capture and next generation sequencing was used to analyze the 73 genes in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1d9cf6a7ff07e0bf6bf72b66492c0d5
https://pubmed.ncbi.nlm.nih.gov/22743793
https://pubmed.ncbi.nlm.nih.gov/22743793
Publikováno v:
Seminars in neurology. 28(2)
Charcot-Marie-Tooth (CMT) disease is caused by mutations in several genes expressed in myelinating Schwann cells and the axons they ensheathe. Typical patients present with distally accentuated motor weakness, muscle wasting, and sensory loss leading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c716983d68e427fdd4e382997457583
https://pubmed.ncbi.nlm.nih.gov/18351520
https://pubmed.ncbi.nlm.nih.gov/18351520
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