Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Haider Katifi"'
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:A40.2-A40
A 37-year old woman with HIV on antiretrovirals (undetectable viral load; CD4 count 520) presented with a painful length dependant sensorimotor polyneuropathy. Investigations showed mild neutropenia, IgA 5.2g/L without paraprotein. Nerve conduction s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7e6e6dfc7a35364b0aecde38c4b6de4
https://doi.org/10.1136/jnnp-2022-abn.128
https://doi.org/10.1136/jnnp-2022-abn.128
Autor:
Louis W. Merton, Chinar Osman, Liam S. Carroll, Christina Petridou, Haider Katifi, Mark Walker
Publikováno v:
Ticks and tick-borne diseases. 11(6)
Lyme neuroborreliosis (LNB) typically presents as a painful radiculitis or a cranial mononeuropathy with lymphocytic meningitis (Bannwarth’s syndrome). Isolated peripheral mononeuropathy or multiple mononeuropathy is less frequently recognised. A 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40449d1307457075539188a70ad5fdfe
https://pubmed.ncbi.nlm.nih.gov/32993951
https://pubmed.ncbi.nlm.nih.gov/32993951
Publikováno v:
International Journal of Case Reports and Images. 13:1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5ac903296fd8ea3782c96ac1fcb5286
https://doi.org/10.5348/101286z01nl2022cr
https://doi.org/10.5348/101286z01nl2022cr
Autor:
Yakov Fellig, Zohar Argov, Leigh B. Waddell, Nicola Foulds, Alexander Lossos, Ingrid Mazanti, Nigel F. Clarke, Olayinka Raheem, Simon Hammans, Haider Katifi, Christopher Lindberg, Bjarne Udd, Anders Oldfors, Homa Tajsharghi, Richard Webster
Publikováno v:
European Journal of Human Genetics. 22:801-808
Myosin myopathies comprise a group of inherited diseases caused by mutations in myosin heavy chain (MyHC) genes. Homozygous or compound heterozygous truncating MYH2 mutations have been demonstrated to cause recessive myopathy with ophthalmoplegia, mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7357f90075b3cd35ef4979b9e82adf
https://doi.org/10.1038/ejhg.2013.250
https://doi.org/10.1038/ejhg.2013.250
Publikováno v:
Neurology. 72(7)
Background: Charcot Marie Tooth (CMT) disease is a heterogeneous group of inherited peripheral motor and sensory neuropathies. CMT4H is an early onset autosomal recessive demyelinating neuropathy. The locus responsible for CMT4H was assigned to chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9886a5384c733ac8292923c8a7ba2ffb
https://pubmed.ncbi.nlm.nih.gov/19221294
https://pubmed.ncbi.nlm.nih.gov/19221294
Publikováno v:
The Lancet. 338:832
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e00f39cbe629fd7d5fe71e5d5f4a0fe
https://doi.org/10.1016/0140-6736(91)90730-d
https://doi.org/10.1016/0140-6736(91)90730-d
Akademický článek
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Autor:
Amy, Ross Russell, Luke, Massey, Imogen, Williams, Mark, Fabian, James, Nicoll, Efrem, Eren, Emmanuela, Pelosi, Martin, Prevett, James, Hell, Haider, Katifi
Publikováno v:
Journal of Neurology, Neurosurgery, & Psychiatry (JNNP); 2018, Vol. 89 Issue: 10 pA41-A41, 1p
Publikováno v:
Journal of the Peripheral Nervous System. Feb2020 Supplement 1, Vol. 25, pS3-S19. 17p.
Autor:
Léger, Jean‐Marc1 jean-marc.leger@aphp.fr, Alfa Cissé, Ousmane2, Cocito, Dario3, Grouin, Jean‐Marie4, Katifi, Haider5, Nobile‐Orazio, Eduardo6, Ouaja, Rabye2, Pouget, Jean7, Rajabally, Yusuf A.8, Sevilla, Teresa9, Merkies, Ingemar S. J.10,11
Publikováno v:
Journal of the Peripheral Nervous System. Mar2019, Vol. 24 Issue 1, p56-63. 8p.