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P Willemsen

Showing results (291-300 of 335) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2021
Neurofilament light chain: A novel blood biomarker in patients with ataxia telangiectasiaS J G Veenhuis, A S Gupta, C M de Gusmão, et al.
Neurology|September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC familiesA Salin-Cantegrel, J-B Rivière, N Dupré, et al.
Placenta|October 19, 2024
First-trimester maternal tryptophan metabolites, utero-placental (vascular)development and hypertensive disorders of pregnancy: The Rotterdam periconceptional cohortSofie K M van Zundert, Michelle Broekhuizen, Mina Mirzaian, et al.
Orphanet Journal of Rare Diseases|July 21, 2023
The most important problems and needs of rasopathy patients with a noonan syndrome spectrum disorderDagmar K Tiemens, Lotte Kleimeier, Erika Leenders, et al.
Fertility and Sterility|August 4, 2020
First effective mHealth nutrition and lifestyle coaching program for subfertile couples undergoing in vitro fertilization treatment: a single-blinded multicenter randomized controlled trialElsje C Oostingh, Maria P H Koster, Matthijs R van Dijk, et al.
Journal of Graduate Medical Education|August 16, 2024
Exploring the Value of an Assessment for the Professional Coaching of ResidentsLara Teheux, Ester H A J Coolen, Brenda van Voorthuizen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Journal of Medical Genetics|March 2, 2019
Genotype-phenotype correlations in ataxia telangiectasia patients with <i>ATM</i> c.3576G>A and c.8147T>C mutationsNienke J H van Os, Luciana Chessa, Corry M R Weemaes, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Cephalalgia : an International Journal of Headache|May 15, 2014
A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhoodClaudia M Weller, Wilhelmina G Leen, Brian G R Neville, et al.
Pageof 34

Showing results (291-300 of 335) with videos related to

Sort By:
Pageof 34
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2021
Neurofilament light chain: A novel blood biomarker in patients with ataxia telangiectasiaS J G Veenhuis, A S Gupta, C M de Gusmão, et al.
Neurology|September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC familiesA Salin-Cantegrel, J-B Rivière, N Dupré, et al.
Placenta|October 19, 2024
First-trimester maternal tryptophan metabolites, utero-placental (vascular)development and hypertensive disorders of pregnancy: The Rotterdam periconceptional cohortSofie K M van Zundert, Michelle Broekhuizen, Mina Mirzaian, et al.
Orphanet Journal of Rare Diseases|July 21, 2023
The most important problems and needs of rasopathy patients with a noonan syndrome spectrum disorderDagmar K Tiemens, Lotte Kleimeier, Erika Leenders, et al.
Fertility and Sterility|August 4, 2020
First effective mHealth nutrition and lifestyle coaching program for subfertile couples undergoing in vitro fertilization treatment: a single-blinded multicenter randomized controlled trialElsje C Oostingh, Maria P H Koster, Matthijs R van Dijk, et al.
Journal of Graduate Medical Education|August 16, 2024
Exploring the Value of an Assessment for the Professional Coaching of ResidentsLara Teheux, Ester H A J Coolen, Brenda van Voorthuizen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Journal of Medical Genetics|March 2, 2019
Genotype-phenotype correlations in ataxia telangiectasia patients with <i>ATM</i> c.3576G>A and c.8147T>C mutationsNienke J H van Os, Luciana Chessa, Corry M R Weemaes, et al.
Journal of Medical Genetics|February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defectsMarjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Cephalalgia : an International Journal of Headache|May 15, 2014
A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhoodClaudia M Weller, Wilhelmina G Leen, Brian G R Neville, et al.
Pageof 34