Zobrazeno 1 - 10
of 363
pro vyhledávání: '"E Holme"'
Autor:
Serina M. Taluja, Brianna L. Cheek, Robert N. Vaughn, Olufemi J. Alabi, John E. Holme, Nisha Jain, David M. Stelly
Publikováno v:
Plant Breeding. 142:238-246
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6045065c9180ec99befad1b6359b47f6
https://doi.org/10.1111/pbr.13081
https://doi.org/10.1111/pbr.13081
Publikováno v:
Acta Neurologica Scandinavica. 92:394-397
We have investigated nine maternal offsprings to patients with a hereditary syndrome of cerebellar ataxia, photomyoclonus, skeletal deformities and lipoma, originally described by Ekbom. The nine family members underwent a thorough neurological exami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e670c711eccd9ee4781bf10c808b4a3
https://doi.org/10.1111/j.1600-0404.1995.tb00153.x
https://doi.org/10.1111/j.1600-0404.1995.tb00153.x
Publikováno v:
Europe PubMed Central
The effect of an early rehabilitation program, including postural training, on ankle joint function after an ankle ligament sprain was investigated prospectively. Ninety-two subjects, matched for age, sex, and level of sports activity, were randomize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2a240b46e9d04c5c6ba0fe1ee34c12
https://doi.org/10.1111/j.1600-0838.1999.tb00217.x
https://doi.org/10.1111/j.1600-0838.1999.tb00217.x
Publikováno v:
Acta Paediatrica. 92:625-628
UNLABELLED In a male patient with hereditary tyrosinaemia type I (HTI), NTBC [2-(2-nitro-4-trifluoro-methylbenzoyl)-1,3-cyclohexandion] treatment and a diet low in phenylalanine and tyrosine were started at the age of 4 wk. At the recommended average
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b047a57e0b94282c68d71e1566f5494
https://doi.org/10.1111/j.1651-2227.2003.tb02518.x
https://doi.org/10.1111/j.1651-2227.2003.tb02518.x
Publikováno v:
The Journal of Headache and Pain
Medication-overuse headache (MOH) is more prevalent among those with low socioeconomic position (SEP), but it is not known how SEP influences the physical and mental health status of people with MOH.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4efecd226dc8cfac8ec26c0bd53b6202
https://doi.org/10.1186/1129-2377-15-s1-b39
https://doi.org/10.1186/1129-2377-15-s1-b39
Publikováno v:
The Journal of Headache and Pain
Methods 129,150 randomly selected individuals aged >16 years were given self-administered questionnaires on general health, headache frequency, over-the-counter (OTC) analgesic use, and health behaviour. Respondents with chronic headache (>15 days/mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2e5062dff746afa4703b0d1e945ff4
https://doi.org/10.1186/1129-2377-15-s1-b38
https://doi.org/10.1186/1129-2377-15-s1-b38
Autor:
N. Lambruschini Ferri, E. Holme, M.aA. Vilaseca Buscà, E. González Pascual, A. Mas Comas, J. Ros Viladoms
Publikováno v:
Anales de Pediatría, Vol 54, Iss 3, Pp 305-309 (2001)
La tirosinemia tipo I es una enfermedad hereditaria autosómica recesiva causada por la actividad deficiente de la enzima fumarilacetoacetasa. El tratamiento con 2-(2-nitro- 4-trifluorometilbenzoil)-1,3-ciclohexadiona (NTBC), un inhibidor del 4-hidro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0808cf7a7f7c66ee446fc0aa1567668e
https://doi.org/10.1016/s1695-4033(01)77531-5
https://doi.org/10.1016/s1695-4033(01)77531-5
Autor:
E. Holme, S. Fletcher, W.S. Hillis, K.L. Woods, Colin R. A. Hewitt, Iain B. Squire, Wendy J. Lawley
Publikováno v:
European Heart Journal. 20:1245-1252
Aims Administration of streptokinase results in an immunological response which may lead to increased risk of anaphylactic reaction or reduced thrombolytic efficacy on repeat administration. For these reasons current recommendations suggest that stre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a920cbec2c53f9a6241fd24913faf416
https://doi.org/10.1053/euhj.1999.1528
https://doi.org/10.1053/euhj.1999.1528
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 56:1129-1132
A 21 month old girl presented with a short history of frequent falls and a right sided foot drop. She went on to suffer recurrent episodes of distal weakness in her arms and legs with hyporeflexia. Electrophysiological studies were consistent with in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dcc93aa4f0a1b869b6007c4f2ff6abe
https://doi.org/10.1136/jnnp.56.10.1129
https://doi.org/10.1136/jnnp.56.10.1129
Autor:
E Holme, Susann Andersson, A K Seyedi Honarvar, Niklas Darin, A R Moslemi, M. Tulinius, A Oldfors, Marita Andersson Grönlund
Publikováno v:
The British journal of ophthalmology. 94(1)
Aim: To describe ophthalmological phenotypes in patients with mitochondrial disease and known genotypes. Methods: A retrospective study was performed on 59 patients (29 male, 30 female) with a mean age of 11.8 years who had mitochondrial disease with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e32186aecba363ec546093ae370b49e1
https://pubmed.ncbi.nlm.nih.gov/20385529
https://pubmed.ncbi.nlm.nih.gov/20385529