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Systematic surveillance cultures as a tool to predict involvement of multidrug antibiotic resistant bacteria in ventilator-associated pneumonia.
- Published in:
- 2008
- By:
- Publication type:
- journal article
National survey of molecular epidemiology of Staphylococcus aureus colonization in Belgian cystic fibrosis patients.
- Published in:
- Journal of Antimicrobial Chemotherapy (JAC), 2007, v. 59, n. 5, p. 893, doi. 10.1093/jac/dkm037
- By:
- Publication type:
- Article
A PATIENT WITH NEONATAL CHOLESTASIS.
- Published in:
- Journal of Mother & Child, 2020, v. 24, n. 4, p. 31, doi. 10.34763/jmotherandchild.20202404.d-20-00012
- By:
- Publication type:
- Article
Mitochondrial abnormalities in myofibrillar myopathies.
- Published in:
- Clinical Neuropathology, 2014, v. 33, n. 2, p. 134, doi. 10.5414/NP300693
- By:
- Publication type:
- Article
The resident microflora of voided midstream urine of healthy controls: standard versus expanded urine culture protocols.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2017, v. 36, n. 4, p. 635, doi. 10.1007/s10096-016-2839-x
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- Publication type:
- Article
Uropathogen distribution and antimicrobial susceptibility in uncomplicated cystitis in Belgium, a high antibiotics prescribing country: 20-year surveillance.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2017, v. 36, n. 1, p. 105, doi. 10.1007/s10096-016-2776-8
- By:
- Publication type:
- Article
Direct susceptibility testing by disk diffusion on clinical samples: a rapid and accurate tool for antibiotic stewardship.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2015, v. 34, n. 6, p. 1207, doi. 10.1007/s10096-015-2349-2
- By:
- Publication type:
- Article
A survey of beta-lactam antibiotics and vancomycin dosing strategies in intensive care units and general wards in Belgian hospitals.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2013, v. 32, n. 6, p. 763, doi. 10.1007/s10096-012-1803-7
- By:
- Publication type:
- Article
Performance evaluation of a modified chromogenic medium, ChromID MRSA New, for the detection of methicillin-resistant Staphylococcus aureus from clinical specimens.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2011, v. 30, n. 12, p. 1595, doi. 10.1007/s10096-011-1265-3
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- Publication type:
- Article
In vitro activity of temocillin against prevalent extended-spectrum beta-lactamases producing Enterobacteriaceae from Belgian intensive care units.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2007, v. 26, n. 11, p. 777, doi. 10.1007/s10096-007-0370-9
- By:
- Publication type:
- Article
Mixed Community-Acquired Fungal Infection in an Apparently Healthy Patient.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2000, v. 19, n. 8, p. 642, doi. 10.1007/s100960000331
- By:
- Publication type:
- Article
Mutans Streptococci, Lactobacilli and Caries Experience in Cystic Fibrosis Homozygotes, Heterozygotes and Healthy Controls.
- Published in:
- Caries Research, 2001, v. 35, n. 6, p. 407, doi. 10.1159/000047483
- By:
- Publication type:
- Article
Elevation of plasma 1-deoxy-sphingolipids in type 2 diabetes mellitus: a susceptibility to neuropathy?
- Published in:
- European Journal of Neurology, 2015, v. 22, n. 5, p. 806, doi. 10.1111/ene.12663
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- Publication type:
- Article
Electromyographie a Inscription Directe.
- Published in:
- Biomedical Engineering / Biomedizinische Technik, 1962, v. 7, n. 2, p. 65, doi. 10.1515/bmte.1962.7.2.65
- By:
- Publication type:
- Article
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Regional variation of Guillain-Barré syndrome.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Hot-spot KIF5A mutations cause familial ALS.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Epilepsy as part of the phenotype associated with ATP1A2 mutations.
- Published in:
- Epilepsia (Series 4), 2008, v. 49, n. 3, p. 500, doi. 10.1111/j.1528-1167.2007.01415.x
- By:
- Publication type:
- Article
Authors' reply.
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 1988, v. 95, n. 10, p. 1083, doi. 10.1111/j.1471-0528.1988.tb06521.x
- By:
- Publication type:
- Article
Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix.
- Published in:
- European Journal of Medical Research, 2017, v. 22, p. 1, doi. 10.1186/s40001-017-0279-4
- By:
- Publication type:
- Article
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?
- Published in:
- Brain & Behavior, 2016, v. 6, n. 4, p. n/a, doi. 10.1002/brb3.451
- By:
- Publication type:
- Article
Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness.
- Published in:
- Skeletal Muscle, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13395-018-0170-1
- By:
- Publication type:
- Article
A tool to facilitate anesthetic preoperative consultations.
- Published in:
- Acta Anaesthesiologica Belgica, 2021, v. 72, p. 113
- By:
- Publication type:
- Article
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness.
- Published in:
- Orphanet Journal of Rare Diseases, 2017, v. 12, p. 1
- By:
- Publication type:
- Article
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Novel genetic and neuropathological insights in neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP).
- Published in:
- 2016
- By:
- Publication type:
- journal article
Novel FHL1 mutation in a family with reducing body myopathy.
- Published in:
- Muscle & Nerve, 2013, v. 47, n. 1, p. 127, doi. 10.1002/mus.23500
- By:
- Publication type:
- Article
Congenital myopathies: an update.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Identification and genotyping of bacteria from paired vaginal and rectal samples from pregnant women indicates similarity between vaginal and rectal microflora.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 7, p. 986, doi. 10.1007/s00415-008-0808-8
- By:
- Publication type:
- Article
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.
- Published in:
- Human Genetics, 2006, v. 118, n. 5, p. 618, doi. 10.1007/s00439-005-0077-x
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- Publication type:
- Article
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03156-3
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- Publication type:
- Article
NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy.
- Published in:
- Acta Neuropathologica Communications, 2022, p. 1, doi. 10.1186/s40478-022-01491-9
- By:
- Publication type:
- Article
Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus–Associated Guillain-Barré Syndrome.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 1, p. 26, doi. 10.1001/jamaneurol.2016.3541
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- Publication type:
- Article
An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease.
- Published in:
- Neuropathology & Applied Neurobiology, 2020, v. 46, n. 4, p. 359, doi. 10.1111/nan.12580
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- Publication type:
- Article
Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with Amyotrophic Lateral Sclerosis.
- Published in:
- Neuropathology & Applied Neurobiology, 2019, v. 45, n. 3, p. 291, doi. 10.1111/nan.12511
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- Publication type:
- Article
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization.
- Published in:
- Neuropathology & Applied Neurobiology, 2011, v. 37, n. 3, p. 271, doi. 10.1111/j.1365-2990.2010.01149.x
- By:
- Publication type:
- Article
Charcot-Marie-Tooth Disease: A Clinico-genetic Confrontation.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 3, p. 416, doi. 10.1111/j.1469-1809.2007.00412.x
- By:
- Publication type:
- Article
Therapeutic drug monitoring-based dose optimisation of piperacillin and meropenem: a randomised controlled trial.
- Published in:
- Intensive Care Medicine, 2014, v. 40, n. 3, p. 380, doi. 10.1007/s00134-013-3187-2
- By:
- Publication type:
- Article
Systematic surveillance cultures as a toolto predict involvement of multidrug antibiotic resistant bacteria in ventilator-associated pneumonia.
- Published in:
- Intensive Care Medicine, 2008, v. 34, n. 4, p. 675, doi. 10.1007/s00134-007-0953-z
- By:
- Publication type:
- Article
Small fiber involvement is independent from clinical pain in late-onset Pompe disease.
- Published in:
- 2022
- By:
- Publication type:
- journal article
SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 12, p. 3634, doi. 10.1093/brain/awt283
- By:
- Publication type:
- Article
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 7, p. 1741, doi. 10.1093/brain/awp115
- By:
- Publication type:
- Article
“Necklace” fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy.
- Published in:
- Acta Neuropathologica, 2009, v. 117, n. 3, p. 283, doi. 10.1007/s00401-008-0472-1
- By:
- Publication type:
- Article
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.
- Published in:
- Acta Neuropathologica, 2009, v. 117, n. 3, p. 293, doi. 10.1007/s00401-008-0479-7
- By:
- Publication type:
- Article
Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 8, p. 1241, doi. 10.1002/acn3.51625
- By:
- Publication type:
- Article
Serum neurofilament heavy chains as early marker of motor neuron degeneration.
- Published in:
- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 10, p. 1971, doi. 10.1002/acn3.50890
- By:
- Publication type:
- Article
Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies.
- Published in:
- Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1200727
- By:
- Publication type:
- Article