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Functional Connectivity of Vermis Correlates with Future Gait Impairments in Parkinson's Disease.
Published in:
Movement Disorders, 2021, v. 36, n. 11, p. 2559, doi. 10.1002/mds.28684
By:
- Maiti, Baijayanta;
- Rawson, Kerri S.;
- Tanenbaum, Aaron B.;
- Koller, Jonathan M.;
- Snyder, Abraham Z.;
- Campbell, Meghan C.;
- Earhart, Gammon M.;
- Perlmutter, Joel S.
Publication type:
Article
Is Levodopa Response a Valid Indicator of Parkinson's Disease?
Published in:
Movement Disorders, 2021, v. 36, n. 4, p. 948, doi. 10.1002/mds.28406
By:
- Martin, W.R. Wayne;
- Miles, Michael;
- Zhong, Qiaonan;
- Hartlein, Johanna;
- Racette, Brad A.;
- Norris, Scott A.;
- Ushe, Mwiza;
- Maiti, Baijayanta;
- Criswell, Susan;
- Davis, Albert A.;
- Kotzbauer, Paul T.;
- Cairns, Nigel J.;
- Perrin, Richard J.;
- Perlmutter, Joel S.
Publication type:
Article
Distinct progression patterns across Parkinson disease clinical subtypes.
Published in:
Annals of Clinical & Translational Neurology, 2021, v. 8, n. 8, p. 1695, doi. 10.1002/acn3.51436
By:
- Myers, Peter S.;
- Jackson, Joshua J.;
- Clover, Amber K.;
- Lessov‐Schlaggar, Christina N.;
- Foster, Erin R.;
- Maiti, Baijayanta;
- Perlmutter, Joel S.;
- Campbell, Meghan C.
Publication type:
Article
Neocortical Lewy Body Pathology Parallels Parkinson's Dementia, but Not Always.
Published in:
Annals of Neurology, 2023, v. 93, n. 1, p. 184, doi. 10.1002/ana.26542
By:
- Martin, W. R. Wayne;
- Younce, John R.;
- Campbell, Meghan C.;
- Racette, Brad A.;
- Norris, Scott A.;
- Ushe, Mwiza;
- Criswell, Susan;
- Davis, Albert A.;
- Alfradique‐Dunham, Isabel;
- Maiti, Baijayanta;
- Cairns, Nigel J.;
- Perrin, Richard J.;
- Kotzbauer, Paul T.;
- Perlmutter, Joel S.
Publication type:
Article
A Clinical Trial of Isradipine: What Went Wrong?
Published in:
2020
By:
- Maiti, Baijayanta;
- Perlmutter, Joel S.
Publication type:
journal article
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Published in:
Nature Medicine, 2015, v. 21, n. 5, p. 537, doi. 10.1038/nm0515-537c
By:
- Wein, Nicolas;
- Vulin, Adeline;
- Falzarano, Maria S;
- Szigyarto, Christina Al-Khalili;
- Maiti, Baijayanta;
- Findlay, Andrew;
- Heller, Kristin N;
- Uhlén, Mathias;
- Bakthavachalu, Baskar;
- Messina, Sonia;
- Vita, Giuseppe;
- Passarelli, Chiara;
- Brioschi, Simona;
- Bovolenta, Matteo;
- Neri, Marcella;
- Gualandi, Francesca;
- Wilton, Steve D;
- Rodino-Klapac, Louise R;
- Yang, Lin;
- Dunn, Diane M
Publication type:
Article
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Published in:
Nature Medicine, 2015, v. 21, n. 4, p. 414, doi. 10.1038/nm0415-414b
By:
- Wein, Nicolas;
- Vulin, Adeline;
- Falzarano, Maria S;
- Szigyarto, Christina Al-Khalili;
- Maiti, Baijayanta;
- Findlay, Andrew;
- Heller, Kristin N;
- Uhlén, Mathias;
- Bakthavachalu, Baskar;
- Messina, Sonia;
- Vita, Giuseppe;
- Passarelli, Chiara;
- Gualandi, Francesca;
- Wilton, Steve D;
- Rodino-Klapac, Louise R;
- Yang, Lin;
- Dunn, Diane M;
- Schoenberg, Daniel R;
- Weiss, Robert B;
- Howard, Michael T
Publication type:
Article
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Published in:
Nature Medicine, 2014, v. 20, n. 9, p. 992, doi. 10.1038/nm.3628
By:
- Wein, Nicolas;
- Vulin, Adeline;
- Falzarano, Maria S;
- Szigyarto, Christina Al-Khalili;
- Maiti, Baijayanta;
- Findlay, Andrew;
- Heller, Kristin N;
- Uhlén, Mathias;
- Bakthavachalu, Baskar;
- Messina, Sonia;
- Vita, Giuseppe;
- Passarelli, Chiara;
- Gualandi, Francesca;
- Wilton, Steve D;
- Rodino-Klapac, Louise R;
- Yang, Lin;
- Dunn, Diane M;
- Schoenberg, Daniel R;
- Weiss, Robert B;
- Howard, Michael T
Publication type:
Article
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
Published in:
Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 452, doi. 10.1093/brain/awn325
By:
- Joachim Schessl;
- Ana L. Taratuto;
- Caroline Sewry;
- Roberta Battini;
- Steven S. Chin;
- Baijayanta Maiti;
- Alberto L. Dubrovsky;
- Marcela G. Erro;
- Graciela Espada;
- Monica Robertella;
- Maria Saccoliti;
- Patricia Olmos;
- Leslie R. Bridges;
- Peter Standring;
- Ying Hu;
- Yaqun Zou;
- Kathryn J. Swoboda;
- Mena Scavina;
- Hans-Hilmar Goebel;
- Christina A. Mitchell
Publication type:
Article
The ZZ Domain of Dystrophin in DMD: Making Sense of Missense Mutations.
Published in:
Human Mutation, 2014, v. 35, n. 2, p. 257, doi. 10.1002/humu.22479
By:
- Vulin, Adeline;
- Wein, Nicolas;
- Strandjord, Dana M.;
- Johnson, Eric K.;
- Findlay, Andrew R.;
- Maiti, Baijayanta;
- Howard, Michael T.;
- Kaminoh, Yuuki J.;
- Taylor, Laura E.;
- Simmons, Tabatha R.;
- Ray, Will C.;
- Montanaro, Federica;
- Ervasti, Jim M.;
- Flanigan, Kevin M.
Publication type:
Article
DMD exon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6.
Published in:
Human Mutation, 2009, v. 30, n. 4, p. 633, doi. 10.1002/humu.20913
By:
- Gurvich, Olga L.;
- Maiti, Baijayanta;
- Weiss, Robert B.;
- Aggarwal, Gaurav;
- Howard, Michael T.;
- Flanigan, Kevin M.
Publication type:
Article
A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy.
Published in:
Human Mutation, 2009, v. 30, n. 3, p. 411, doi. 10.1002/humu.20879
By:
- Maiti, Baijayanta;
- Arbogast, Sandrine;
- Allamand, Valérie;
- Moyle, Mark W.;
- Anderson, Christine B.;
- Richard, Pascale;
- Guicheney, Pascale;
- Ferreiro, Ana;
- Flanigan, Kevin M.;
- Howard, Michael T.
Publication type:
Article
Emergent Functional Network Effects in Parkinson Disease.
Published in:
Cerebral Cortex, 2019, v. 29, n. 6, p. 2509, doi. 10.1093/cercor/bhy121
By:
- Gratton, Caterina;
- Koller, Jonathan M;
- Shannon, William;
- Greene, Deanna J;
- Maiti, Baijayanta;
- Snyder, Abraham Z;
- Petersen, Steven E;
- Perlmutter, Joel S;
- Campbell, Meghan C
Publication type:
Article
Emergent Functional Network Effects in Parkinson Disease.
Published in:
Cerebral Cortex, 2019, v. 29, n. 4, p. 1701, doi. 10.1093/cercor/bhy229
By:
- Gratton, Caterina;
- Koller, Jonathan M;
- Shannon, William;
- Greene, Deanna J;
- Maiti, Baijayanta;
- Snyder, Abraham Z;
- Petersen, Steven E;
- Perlmutter, Joel S;
- Campbell, Meghan C
Publication type:
Article
PET Quantification of [<sup>18</sup>F]VAT in Human Brain and Its Test-Retest Reproducibility and Age Dependence.
Published in:
Journal of Nuclear Medicine, 2024, v. 65, n. 8, p. 1, doi. 10.2967/jnumed.123.266860
By:
- O'Donnell, John L.;
- Soda, Anil Kumar;
- Hao Jiang;
- Norris, Scott A.;
- Maiti, Baijayanta;
- Karimi, Morvarid;
- Campbell, Meghan C.;
- Moerlein, Stephen M.;
- Zhude Tu;
- Perlmutter, Joel S.
Publication type:
Article
PET Quantification of [<sup>18</sup>F]VAT in Human Brain and Its Test-Retest Reproducibility and Age Dependence.
Published in:
Journal of Nuclear Medicine, 2024, v. 65, n. 6, p. 956, doi. 10.2967/jnumed.123.266860
By:
- O'Donnell, John L.;
- Soda, Anil Kumar;
- Hao Jiang;
- Norris, Scott A.;
- Maiti, Baijayanta;
- Karimi, Morvarid;
- Campbell, Meghan C.;
- Moerlein, Stephen M.;
- Tu, Zhude;
- Perlmutter, Joel S.
Publication type:
Article
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
Published in:
2008
By:
- Schessl, Joachim;
- Yaqun Zou;
- McGrath, Meagan J.;
- Cowling, Belinda S.;
- Maiti, Baijayanta;
- Chin, Steven S.;
- Sewry, Caroline;
- Battini, Roberta;
- Ying Hu;
- Cottle, Denny L.;
- Rosenblatt, Michael;
- Spruce, Lynn;
- Ganguly, Arupa;
- Kirschner, Janbernd;
- Judkins, Alexander R.;
- Golden, Jeffrey A.;
- Goebel, Hans-Hilmar;
- Muntoni, Francesco;
- Flanigan, Kevin M.;
- Mitchell, Christina A.
Publication type:
journal article

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