All papers authored by Dimah Saade
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Rita Volochayev,
Bianca Russell ,
Adrian Rodriguez,
Steven A. Moore ,
Ning Chang ,
Natalie D. Shaw,
Kaoru Inoue ,
Angela Delaney,
Ying Hu,
Sandra Donkervoort,
B. Jeanne Billioux,
Brooke Meader,
Chamindra G. Konersman,
Payam Mohassel
and 7 other authors
Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants
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Eduardo Paredes,
Victoria Biancavilla,
Sandra Donkervoort,
Rupleen Kaur,
Tanya Lehky,
Margaret Fink,
Diane Armao,
Steven J. Gray,
Melissa Waite,
Sarah Debs ,
Gilberto Averion ,
Ying Hu
and 4 other authors
Giant axonal neuropathy: cross-sectional analysis of a large natural history cohort
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,
Sandra Donkervoort,
Museer A. Lone,
Matthew Nalls,
Kenneth Gable ,
Sita D. Gupta ,
A. Reghan Foley,
Ying Hu,
Jonas Alex Morales Saute,
Ana Lucila Moreira,
Fernando Kok,
Alessandro Introna ,
Giancarlo Logroscino ,
Christopher Grunseich,
Alec R. Nickolls
and 31 other authors
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis
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Micaela McCall,
Megan L. Bradson,
Marcin Szczot,
Mark H. Pitcher,
Nima Ghitani,
Eleni Frangos ,
Jonathan Cole,
Diana Bharucha-Goebel,
Dimah Saade ,
Tracy Ogata
and 6 other authors
Innocuous pressure sensation requires A-type afferents but not functional ΡΙΕΖΟ2 channels in humans
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Teerin Liewluck,
Ying Hu,
Daniel Ezzo,
Tracy Ogata,
Dimah Saade ,
Sarah Neuhaus,
Véronique Bolduc,
Yaqun Zou,
Sandra Donkervoort,
Livija Medne,
Charlotte J. Sumner,
P. James B. Dyck,
P. James B. Dyck,
Klaas J. Wierenga
and 9 other authors
Dominant collagen XII mutations cause a distal myopathy
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Andrew G. Marshall ,
Adarsh Makdani ,
Ewa Jarocka,
Jaquette Liljencrantz ,
Mikael Ridderström ,
Sumaiya Shaikh,
Francis O’Neill ,
Dimah Saade ,
Sandra Donkervoort,
A. Reghan Foley,
Jan Minde ,
Mats Trulsson,
Jonathan Cole ,
Carsten G. Bönnemann
and 4 other authors
An ultrafast system for signaling mechanical pain in human skin
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Ying Hu,
Véronique Bolduc,
Katherine Ru-Yui Chao,
Julián Nevado,
Ana Lamuedra,
Raquel Largo ,
Gabriel Herrero-Beaumont
and 15 other authors
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
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Farrar,
J. K. Goodrich
and 38 other authors
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
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Jaquette Liljencrantz ,
Nima Ghitani ,
Arnab Barik ,
Ruby Lam ,
James H. Thompson ,
Diana Bharucha-Goebel,
Dimah Saade ,
Aaron Necaise,
Sandra Donkervoort,
A. Reghan Foley,
Taylor Gordon,
Laura Case ,
M. Catherine Bushnell,
Carsten G. Bönnemann
and 1 other authors
PIEZO2 mediates injury-induced tactile pain in mice and humans
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Mary O. Cox,
Tahseen Mozaffar,
Mena Scavina,
Vikki A. Stefans,
Thomas L. Winder,
Kevin P. Campbell ,
Steven A. Moore,
Katherine D. Mathews
GMPPB -Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation
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