Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Albert J. Tahmoush"'
Autor:
Teepu Siddique, Albert J. Tahmoush, Faisal Fecto, Irfan Lalani, Han Xiang Deng, Kaouther Ajroud, Vamsi K. Mootha, Sarah E. Calvo, Senda Ajroud-Driss, Terry Heiman-Patterson, Nailah Siddique
Publikováno v:
neurogenetics. 16:1-9
Mitochondrial myopathies belong to a larger group of systemic diseases caused by morphological or biochemical abnormalities of mitochondria. Mitochondrial disorders can be caused by mutations in either the mitochondrial or nuclear genome. Only 5 % of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd171098e4126976e4e35ede6e239f4
https://doi.org/10.1007/s10048-014-0421-1
https://doi.org/10.1007/s10048-014-0421-1
Publikováno v:
The Clinical Journal of Pain. 16:340-344
OBJECTIVE Patients with complex regional pain syndrome type I (CRPSD1) may have thermal allodynia after application of a non-noxious thermal stimulus to the affected limb. We measured the warm, cold, heat-evoked pain threshold and the cold-evoked pai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3143f829add58e2145fa5e491b17dfba
https://doi.org/10.1097/00002508-200012000-00011
https://doi.org/10.1097/00002508-200012000-00011
Publikováno v:
Muscle & Nerve. 23:1736-1747
Paramyotonia congenita (PC) is an autosomal-dominant disorder due to a point mutation in the adult skeletal muscle Na channel gene. Muscle fibers from PC patients have normal membrane properties at 32 degrees C. At 27 degrees C, they are inexcitable,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cdbd3ab4eadd1adc5fb34ea2b1d4a5e
https://doi.org/10.1002/1097-4598(200011)23:11<1736::aid-mus10>3.0.co
https://doi.org/10.1002/1097-4598(200011)23:11<1736::aid-mus10>3.0.co
Autor:
Zohar Argov, William J. Bank, Bernadette Kalman, Albert J. Tahmoush, Hansjuerg Alder, Salvatore DiMauro, Terry Heiman-Patterson, Jeffrey M. Chavin
Publikováno v:
Muscle & Nerve. 20:1219-1224
We present a family with severe exercise intolerance, progressive proximal weakness, and lactic acidemia. Fifteen of 24 family members in five generations were affected. Since the affected males do not have offspring at this time, the family pedigree
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9b7e9c68ff9db50e7748bc5ba168f95
https://doi.org/10.1002/(sici)1097-4598(199710)20:10<1219::aid-mus2>3.0.co
https://doi.org/10.1002/(sici)1097-4598(199710)20:10<1219::aid-mus2>3.0.co
Publikováno v:
Journal of the Neurological Sciences. 128:175-180
Fourteen patients were identified with (1) pain and sensory changes in a brachial plexus distribution, (2) aggravation of pain with use of the affected extremity, and (3) pain on palpation over the brachial plexus. All patients had minimal or no intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::480c1e5e22b40cc0c8df11701241c438
https://doi.org/10.1016/0022-510x(94)00220-i
https://doi.org/10.1016/0022-510x(94)00220-i
Autor:
Preston E. Thompson, Terry Heiman-Patterson, Thomas Krupa, Albert J. Tahmoush, Eduardo Nobile-Orazio, Michael E. Shy
Publikováno v:
Journal of the Neurological Sciences. 120:38-45
IgM M-proteins in some motor neuron disease (MND) patients bind immunologically to shared determinants on gangliosides GM1 and GD1b. Since patients with these M-proteins have improved with immunotherapy the antibodies may be important in the pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d849a4aaf533d272e48077b9667988
https://doi.org/10.1016/0022-510x(93)90022-q
https://doi.org/10.1016/0022-510x(93)90022-q
Publikováno v:
Journal of the Neurological Sciences. 155:208-210
Although swallowing difficulties (dysphagia) frequently occur in acute brainstem infarction, physiological studies of dysphagia (videofluoroscopy, manometry) are rarely reported. We present a patient with ipsilateral Horner's syndrome, palatal and la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd81463b970c9e3c2505894b537cb1f9
https://doi.org/10.1016/s0022-510x(97)00307-9
https://doi.org/10.1016/s0022-510x(97)00307-9
Publikováno v:
Muscle & Nerve. 18:475-477
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c225d665e7867fc45aa2e78e131415
https://doi.org/10.1002/mus.880180419
https://doi.org/10.1002/mus.880180419
Autor:
Albert J, Tahmoush, Mary S, Amir, William W, Connor, James K, Farry, Sevastian, Didato, Alice, Ulhoa-Cintra, Jennifer M, Vasas, Robert J, Schwartzman, Harold L, Israel, Herbert, Patrick
Publikováno v:
Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG. 19(3)
To redefine the utility of CSF-ACE as a selective indicator of probable CNS neurosarcoidosis.The diagnosis of probable CNS neurosarcoidosis required: (a) biopsy evidence of systemic sarcoidosis, (b) cortical, brainstem, and/or spinal cord deficits, (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d8eca7331ed28aa034e0d498590432e
https://pubmed.ncbi.nlm.nih.gov/12405488
https://pubmed.ncbi.nlm.nih.gov/12405488
Publikováno v:
Journal of the neurological sciences. 150(2)
We performed a retrospective study of 29 patients with CRPS1 (RSD) who were initially examined between 1983 and 1993, and had either transthoracic (lower third of stellate ganglia to T3) or lumbar (L2-L4) sympathectomy. The patients were followed fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::941767aa4549b0473a24b39f3aaa242f
https://pubmed.ncbi.nlm.nih.gov/9268243
https://pubmed.ncbi.nlm.nih.gov/9268243