Gabriel Miltenberger-Miltenyi
AuthID: R-000-VAB
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TÃTULO: Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea-Acanthocytosis Full Text
AUTORES: Miltenberger Miltenyi, G; Jones, A; Tetlow, AM; Conceição, VA; Crary, JF; Ditzel, RM; ; Farrell, K; Nandakumar, R; Barton, B; Karp, BI; Kirby, A; Lett, DJ; Mente, K; Morgello, S; Simon, DK; Walker, RH;
PUBLICAÇÃO: 2023, FONTE: MOVEMENT DISORDERS
AUTORES: Miltenberger Miltenyi, G; Jones, A; Tetlow, AM; Conceição, VA; Crary, JF; Ditzel, RM; ; Farrell, K; Nandakumar, R; Barton, B; Karp, BI; Kirby, A; Lett, DJ; Mente, K; Morgello, S; Simon, DK; Walker, RH;
PUBLICAÇÃO: 2023, FONTE: MOVEMENT DISORDERS
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TÃTULO: Increased monohexosylceramide levels in the serum of established rheumatoid arthritis patients
AUTORES: Miltenberger Miltenyi, G; Cruz Machado, AR; Saville, J; Conceicao, VA; Calado, A; Lopes, I; Fuller, M; Fonseca, JE;
PUBLICAÇÃO: 2020, FONTE: RHEUMATOLOGY, VOLUME: 59, NÚMERO: 8
AUTORES: Miltenberger Miltenyi, G; Cruz Machado, AR; Saville, J; Conceicao, VA; Calado, A; Lopes, I; Fuller, M; Fonseca, JE;
PUBLICAÇÃO: 2020, FONTE: RHEUMATOLOGY, VOLUME: 59, NÚMERO: 8
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TÃTULO: C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
AUTORES: Miltenberger Miltenyi, G; Conceicao, VA; Gromicho, M; Pronto Laborinho, AC; Pinto, S; Andersen, PM; de Carvalho, M;
PUBLICAÇÃO: 2019, FONTE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 90, NÚMERO: 1
AUTORES: Miltenberger Miltenyi, G; Conceicao, VA; Gromicho, M; Pronto Laborinho, AC; Pinto, S; Andersen, PM; de Carvalho, M;
PUBLICAÇÃO: 2019, FONTE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 90, NÚMERO: 1
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TÃTULO: C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis Full Text
AUTORES: Gabriel Miltenberger Miltenyi; Vasco A Conceicao; Marta Gromicho; Ana Catarina Pronto Laborinho; Susana Pinto ; Peter M Andersen; Mamede De Carvalho;
PUBLICAÇÃO: 2019, FONTE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, NÚMERO: 26
AUTORES: Gabriel Miltenberger Miltenyi; Vasco A Conceicao; Marta Gromicho; Ana Catarina Pronto Laborinho; Susana Pinto ; Peter M Andersen; Mamede De Carvalho;
PUBLICAÇÃO: 2019, FONTE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, NÚMERO: 26
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TÃTULO: Genetic polymorphisms of proangiogenic factors seem to favor hepatocellular carcinoma development in alcoholic cirrhosis
AUTORES: Mariana V Machado; Andre Janeiro; Gabriel Miltenberger Miltenyi; Helena Cortez Pinto;
PUBLICAÇÃO: 2014, FONTE: EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, VOLUME: 26, NÚMERO: 4
AUTORES: Mariana V Machado; Andre Janeiro; Gabriel Miltenberger Miltenyi; Helena Cortez Pinto;
PUBLICAÇÃO: 2014, FONTE: EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, VOLUME: 26, NÚMERO: 4
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TÃTULO: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration Full Text
AUTORES: Julie van der Zee; Tim Van Langenhove; Gabor G Kovacs; Lubina Dillen; William Deschamps; Sebastiaan Engelborghs; Radoslav Matej; Mathieu Vandenbulcke; Anne Sieben; Bart Dermaut; Katrien Smets; Philip Van Damme; Celine Merlin; Annelies Laureys; Marleen Van Den Broeck; Maria Mattheijssens; Karin Peeters; Luisa Benussi; Giuliano Binetti; Roberta Ghidoni; ...Mais
PUBLICAÇÃO: 2014, FONTE: ACTA NEUROPATHOLOGICA, VOLUME: 128, NÚMERO: 3
AUTORES: Julie van der Zee; Tim Van Langenhove; Gabor G Kovacs; Lubina Dillen; William Deschamps; Sebastiaan Engelborghs; Radoslav Matej; Mathieu Vandenbulcke; Anne Sieben; Bart Dermaut; Katrien Smets; Philip Van Damme; Celine Merlin; Annelies Laureys; Marleen Van Den Broeck; Maria Mattheijssens; Karin Peeters; Luisa Benussi; Giuliano Binetti; Roberta Ghidoni; ...Mais
PUBLICAÇÃO: 2014, FONTE: ACTA NEUROPATHOLOGICA, VOLUME: 128, NÚMERO: 3
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TÃTULO: Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation
AUTORES: Catarina Chester; Mamede de Carvalho ; Gabriel Miltenberger; Sonia Pereira; Lubina Dillen; Julie van der Zee; Christine van Broeckhoven; Alexandre de Mendonca ;
PUBLICAÇÃO: 2013, FONTE: AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, VOLUME: 14, NÚMERO: 1
AUTORES: Catarina Chester; Mamede de Carvalho ; Gabriel Miltenberger; Sonia Pereira; Lubina Dillen; Julie van der Zee; Christine van Broeckhoven; Alexandre de Mendonca ;
PUBLICAÇÃO: 2013, FONTE: AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, VOLUME: 14, NÚMERO: 1
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TÃTULO: AFM based-force spectroscopy as a functional diagnostic nanotool for hematological diseases Full Text
AUTORES: Carvalho, FA; Tavares, A; Teodoro, M; Miltenberger Miltenyi, G; Santos, NC ;
PUBLICAÇÃO: 2013, FONTE: 9th European-Biophysical-Societies-Association Congress in EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, VOLUME: 42
AUTORES: Carvalho, FA; Tavares, A; Teodoro, M; Miltenberger Miltenyi, G; Santos, NC ;
PUBLICAÇÃO: 2013, FONTE: 9th European-Biophysical-Societies-Association Congress in EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, VOLUME: 42
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TÃTULO: Phenotypic variability of familial and sporadic progranulin p.Gln257ProfsX27 mutation Full Text
AUTORES: Pires, C; Coelho, M; Valadas, A; Barroso, C; Miltenberger Miltenyi, G; Pimentel, J; Duyckaerts, C; de Mendonca, A; Verdelho, A;
PUBLICAÇÃO: 2013, FONTE: JOURNAL OF NEUROLOGY, VOLUME: 260
AUTORES: Pires, C; Coelho, M; Valadas, A; Barroso, C; Miltenberger Miltenyi, G; Pimentel, J; Duyckaerts, C; de Mendonca, A; Verdelho, A;
PUBLICAÇÃO: 2013, FONTE: JOURNAL OF NEUROLOGY, VOLUME: 260
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TÃTULO: Double hit for the neurons: the coexistence of a novel presenilin 2 mutation and a huntingtin gene CAG repeat expansion Full Text
AUTORES: Remenyi, V; Miltenberger Miltenyi, G; Nyiro, G; Kovacs, T; Molnar, MJ;
PUBLICAÇÃO: 2012, FONTE: 22nd Meeting of the European-Neurological-Society in JOURNAL OF NEUROLOGY, VOLUME: 259
AUTORES: Remenyi, V; Miltenberger Miltenyi, G; Nyiro, G; Kovacs, T; Molnar, MJ;
PUBLICAÇÃO: 2012, FONTE: 22nd Meeting of the European-Neurological-Society in JOURNAL OF NEUROLOGY, VOLUME: 259
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