Výsledky vyhledávání - "Jikke-Mien F. Niermeijer"

Evaluation of management and guideline adherence in children with mild traumatic brain injury

Autor: Irene A.W. Kotsopoulos, Merel C. Broers, Jos F.M. Bruinenberg, Coriene E. Catsman-Berrevoets, Jikke-Mien F. Niermeijer, Hester F. Lingsma

Publikováno v: Brain Injury, 32(8), 1028-1039. Informa Healthcare

Aim: To evaluate the management and guideline adherence in children with mild traumatic brain injury (MTBI) in emergency departments (ED) in the Netherlands. Methods: A multicentre cohort study was conducted, including children younger than 18 years

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c953793a6c3eba564f11b3034e2cf3f4
https://pure.eur.nl/en/publications/aa93265b-2fe1-4a7a-9099-22e797baeb02

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Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum

Autor: Jikke-Mien F. Niermeijer, Hans Juergen Christen, Johan L.K. Van Hove, Bwee Tien Poll-The, Curtis R. Coughlin, Hans Hartmann, Jost Wigand Richter, Sylvia Stockler-Ipsiroglu, Renata C. Gallagher, Clara D.M. van Karnebeek, Aisha Ghani, Sylvia A. Tiebout

Publikováno v: Pediatric Neurology. 59:6-12

Background Pyridoxine-dependent epilepsy is a rare autosomal recessive epileptic encephalopathy caused by antiquitin ( ALDH7A1 ) deficiency. In spite of adequate seizure control, 75% of patients suffer intellectual developmental disability. Antiquiti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6594022fa2bb206ddf88395d4b133d72
https://doi.org/10.1016/j.pediatrneurol.2015.12.013

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Correlation Between Clinical and Histologic Findings in the Human Neonatal Hippocampus After Perinatal Asphyxia

Autor: Eleonora Aronica, Timo R. de Haan, J.H. Koelman, Liesbeth Reneman, Charles B. L. M. Majoie, Jikke-Mien F. Niermeijer, Irene A.M. Schiering

Publikováno v: Journal of neuropathology and experimental neurology, 73(4), 324-334. Lippincott Williams and Wilkins
Journal of Neuropathology and Experimental Neurology, 73(4), 324-334. Lippincott Williams & Wilkins

Hypoxic ischemic encephalopathy after perinatal asphyxia is a major cause of mortality and morbidity in infants. Here, we evaluated pathologic changes in the hippocampi of a cohort of 16 deceased full-term asphyxiated infants who died from January 20

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e172ba98baddae2f9c3c0985e8a888e6
https://doi.org/10.1097/nen.0000000000000056

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Propofol in status epilepticus: little evidence, many dangers?

Autor: Cees A. van Donselaar, Cuno S P M Uiterwaal, Jikke-Mien F. Niermeijer

Publikováno v: Journal of neurology, 250(10), 1237-1240. D. Steinkopff-Verlag

Several guidelines recommend the use of propofol for the treatment of refractory status epilepticus. An increased mortality rate in high dose, long-term treatment with propofol in adult patients was published recently. This prompted us to assess the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5c4a0183610b0b171c0c63783d19a21
https://doi.org/10.1007/s00415-003-0180-7

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Fc gamma receptor IIIA genotype is associated with rituximab response in antimyelin-associated glycoprotein neuropathy

Autor: Raymond D. Schellevis, Jeanette H. W. Leusen, Jikke-Mien F Niermeijer, W-Ludo van der Pol, Nicolette C. Notermans, Leonard H. van den Berg, Maaike Nederend, Abraham C. J. Stork

Publikováno v: Journal of neurology, neurosurgery, and psychiatry, 85(8), 916-918. BMJ Publishing Group

Background Treatment with anti-B cell antibody rituximab may ameliorate the disease course in a subgroup of patients with polyneuropathy associated with IgM monoclonal gammopathy. Polymorphisms of leukocyte IgG receptors (Fc gamma R) that influence e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e98a6bd812371a354074149e4dcfa30
https://pure.amc.nl/en/publications/fc-gamma-receptor-iiia-genotype-is-associated-with-rituximab-response-in-antimyelinassociated-glycoprotein-neuropathy(0856d539-91c9-4868-8c36-5f844d29df5b).html

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EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases, 9(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol. 9 (2014) P. 23

BACKGROUND: Pontocerebellar hypoplasia (PCH) represents a group of neurodegenerative disorders with prenatal onset. Eight subtypes have been described thus far (PCH1-8) based on clinical and genetic features. Common characteristics include hypoplasia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c44be1d4ac832b4fbeddf70fd1e155
https://pubmed.ncbi.nlm.nih.gov/24524299

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