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Gabriel Miltenberger-Miltenyi

Showing results (11-20 of 37) with videos related to

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Revista Portuguesa De Cardiologia|September 17, 2019
Post mortem genetic test, the clinical diagnosis is not fade with the death of the patientSílvia Ribeiro, Luís Coelho, Katerina Puentes, et al.
Archives of Neurology|July 11, 2007
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL geneGabriel Miltenberger-Miltenyi, Andreas R Janecke, Julia V Wanschitz, et al.
Bone|July 17, 2012
Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of boneLaëtitia Michou, Natércia Conceição, Jean Morissette, et al.
ACS Nano|August 25, 2010
Atomic force microscopy-based molecular recognition of a fibrinogen receptor on human erythrocytesFilomena A Carvalho, Simon Connell, Gabriel Miltenberger-Miltenyi, et al.
Rheumatology (Oxford, England)|December 7, 2019
Increased monohexosylceramide levels in the serum of established rheumatoid arthritis patientsGabriel Miltenberger-Miltenyi, Ana Rita Cruz-Machado, Jennifer Saville, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 15, 2017
International Survey of ALS Experts about Critical Questions for Assessing Patients with ALSMamede De Carvalho, Adam Ryczkowski, Peter Andersen, et al.
International Journal of Molecular Sciences|September 23, 2022
Serum Phospholipid Profile Changes in Gaucher Disease and Parkinson's DiseaseLaura López de Frutos, Francisco Almeida, Jessica Murillo-Saich, et al.
Journal of Alzheimer'S Disease : JAD|July 2, 2013
Phenotypic variability of familial and sporadic Progranulin p.Gln257Profs*27 mutationCarolina Pires, Miguel Coelho, Anabela Valadas, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|September 5, 2022
Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotypeMargarida Oliveira, Olga Azevedo, Bebiana Faria, et al.
Revista Portuguesa De Cardiologia|January 6, 2020
Screening for Fabry disease in patients with left ventricular noncompactionOlga Azevedo, Nuno Marques, Nuno Craveiro, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Revista Portuguesa De Cardiologia|September 17, 2019
Post mortem genetic test, the clinical diagnosis is not fade with the death of the patientSílvia Ribeiro, Luís Coelho, Katerina Puentes, et al.
Archives of Neurology|July 11, 2007
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL geneGabriel Miltenberger-Miltenyi, Andreas R Janecke, Julia V Wanschitz, et al.
Bone|July 17, 2012
Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of boneLaëtitia Michou, Natércia Conceição, Jean Morissette, et al.
ACS Nano|August 25, 2010
Atomic force microscopy-based molecular recognition of a fibrinogen receptor on human erythrocytesFilomena A Carvalho, Simon Connell, Gabriel Miltenberger-Miltenyi, et al.
Rheumatology (Oxford, England)|December 7, 2019
Increased monohexosylceramide levels in the serum of established rheumatoid arthritis patientsGabriel Miltenberger-Miltenyi, Ana Rita Cruz-Machado, Jennifer Saville, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 15, 2017
International Survey of ALS Experts about Critical Questions for Assessing Patients with ALSMamede De Carvalho, Adam Ryczkowski, Peter Andersen, et al.
International Journal of Molecular Sciences|September 23, 2022
Serum Phospholipid Profile Changes in Gaucher Disease and Parkinson's DiseaseLaura López de Frutos, Francisco Almeida, Jessica Murillo-Saich, et al.
Journal of Alzheimer'S Disease : JAD|July 2, 2013
Phenotypic variability of familial and sporadic Progranulin p.Gln257Profs*27 mutationCarolina Pires, Miguel Coelho, Anabela Valadas, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|September 5, 2022
Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotypeMargarida Oliveira, Olga Azevedo, Bebiana Faria, et al.
Revista Portuguesa De Cardiologia|January 6, 2020
Screening for Fabry disease in patients with left ventricular noncompactionOlga Azevedo, Nuno Marques, Nuno Craveiro, et al.
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