All papers authored by Michael Kruer
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Somayeh Bakhtiari,
Jacob Forstrom,
Allan Bayat ,
Frédéric Bilan ,
Gwenaël Le Guyader,
Ebba Alkhunaizi ,
Hilary Vernon ,
Sergio R. Padilla-Lopez,
Michael C. Kruer
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Sheetal Shetty,
Sean Gamble,
Jennifer Heim,
Ningning Zhao,
Gideon Stitt,
Matthew Pankratz,
Tara Mangum,
Iris Marku,
Robert B. Rosenberg,
Angus A. Wilfong,
Michael C. Fahey,
Sukhan Kim,
Scott J. Myers,
Brian Appavu
and 1 other authors
Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation
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Luis A. Pérez-Jurado,
María Palomares,
Sneha Rangu ,
Sarah E. Sheppard ,
Wendy K. Chung ,
Michael C. Kruer ,
Mira Kharbanda ,
David J. Amor ,
George McGillivray ,
Julie S. Cohen ,
Sixto García-Miñaúr,
Clare L. van Eyk ,
Kelly Harper,
Lachlan A. Jolly
and 60 other authors
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Kyung Ah Han,
Dongwook Kim,
Gyubin Jang,
Somayeh Bakhtiari,
Dongseok Lim,
Hee Young Kim,
Jinhu Kim,
Hyeonho Kim,
Julia Wynn,
Wendy K. Chung,
Giuseppina Vitiello,
Ioana Cutcutache,
Matthew Page,
Jozef Gecz
and 25 other authors
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Michael C. Fahey,
Gareth Baynam,
Jozef Gécz,
Nadia Badawi,
Sarah McIntyre
Common data elements to standardize genomics studies in cerebral palsy
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J. Pedro Fernández-Murray ,
Mahtab Tavasoli ,
Heinrich Sticht ,
Gisela Stoltenburg-Didinger ,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla ,
Katta Mohan Girisha ,
Dhanya Lakshmi Narayanan ,
Parneet Kaur
and 14 other authors
Bi-allelic variants inCHKAcause a neurodevelopmental disorder with epilepsy and microcephaly
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J. Pedro Fernandez Murray,
Mahtab Tavasoli,
Heinrich Sticht,
Gisela Stoltenburg-Didinger,
Leila Motlagh Scholle ,
Somayeh Bakhtiari,
Michael C. Kruer ,
Hossein Darvish,
Saghar Ghasemi Firouzabadi ,
Alex Pagnozzi,
Anju Shukla,
Katta Mohan Girisha,
Dhanya Lakshmi Narayanan,
Parneet Kaur
and 14 other authors
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly
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Opsoclonus–myoclonus–ataxia syndrome in children
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Sara A. Lewis ,
Somayeh Bakhtiari,
Xue Zeng ,
Michael C. Sierant ,
Sheetal Shetty,
Sandra M. Nordlie ,
Aureliane Elie,
Mark A. Corbett ,
Bethany Y. Norton,
Clare L. van Eyk ,
Shozeb Haider ,
Brandon S. Guida,
Helen Magee,
James Liu
and 62 other authors
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Download from www.nature.com
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Sara A. Lewis ,
Somayeh Bakhtiari,
Xue Zeng ,
Michael C. Sierant ,
Sheetal Shetty,
Sandra M. Nordlie ,
Aureliane Elie,
Mark A. Corbett ,
Bethany Y. Norton,
Clare L. van Eyk ,
Shozeb Haider ,
Brandon S. Guida,
Helen Magee,
James Liu
and 62 other authors
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
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Michael C. Kruer ,
Aleksandar Videnovic,
Amy Robichaux‐Viehoever,
Laura Swett,
Dennis A. Revicki ,
Randall H. Bender,
William R. Lenderking
A Scale to Assess Activities of Daily Living in Pantothenate Kinase‐Associated Neurodegeneration
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