P. Mohassel
发表
Courtney E. French,
F. Muntoni,
M. Tarnopolsky,
2021,
medRxiv.
Beryl B. Cummings,
Stephane E. Castel,
Paul J. Hoffman,
2019,
Science.
Beryl B. Cummings,
Jamie L. Marshall,
D. MacArthur,
2018,
Annals of neurology.
A. Mammen,
P. Mohassel,
2013,
Muscle & nerve.
A. Arai,
C. Bönnemann,
S. Donkervoort,
2020,
Neuromuscular Disorders.
D. Goldstein,
A. Allen,
T. Strom,
2018,
The EMBO journal.
W. Stenzel,
A. Hentschel,
C. Preusse,
2022,
Genes.
M. Fotuhi,
H. Wengreen,
P. Mohassel,
2009
.
A. Mammen,
P. Mohassel,
2018,
Journal of neuromuscular diseases.
E. Shoubridge,
T. Hornemann,
Mari J Aaltonen,
2022,
The Journal of clinical investigation.
E. Shoubridge,
T. Hornemann,
Mari J Aaltonen,
2022,
bioRxiv.
C. Bönnemann,
S. Donkervoort,
A. Foley,
2020,
BMC Pediatrics.
Colleen E. Wahl,
A. Mammen,
C. Toro,
2018,
Neurology: Neuroimmunology & Neuroinflammation.
Jamie L. Marshall,
D. MacArthur,
M. Lek,
2019,
Journal of neuromuscular diseases.
C. Bönnemann,
W. Zein,
A. Hoke,
2017,
Neurology: Genetics.
L. Mesrob,
B. Banwell,
E. Malfatti,
2017,
Neuromuscular Disorders.
A. Mammen,
P. Mohassel,
2013,
Current opinion in rheumatology.
C. Bönnemann,
D. Bharucha-Goebel,
S. Donkervoort,
2016,
Journal of child neurology.
C. Bönnemann,
D. Bharucha-Goebel,
S. Donkervoort,
2016
.
K. Yaffe,
M. Fotuhi,
P. Mohassel,
2009,
Nature Clinical Practice Neurology.
C. Bönnemann,
D. Bharucha-Goebel,
S. Donkervoort,
2017,
Neuromuscular Disorders.
M. Cookson,
C. Bönnemann,
M. Santi,
2021,
Annals of clinical and translational neurology.
T. Siddique,
S. Coppens,
P. Handford,
2021,
American journal of human genetics.
Beryl B. Cummings,
Paul J. Hoffman,
D. MacArthur,
2019,
bioRxiv.
W. Chung,
Yufeng Shen,
C. Tifft,
2016,
Journal of Medical Genetics.
Courtney E. French,
F. Muntoni,
M. Tarnopolsky,
2022,
Nature Communications.
C. Bönnemann,
P. Mohassel,
2015
.
T. Hornemann,
Sita D Gupta,
K. Gable,
2021,
Nature Medicine.
Janice S. Lee,
M. Leppert,
F. Collins,
2017,
Nature Communications.
M. Young,
V. Kram,
C. Bonnemann,
2020,
Scientific Reports.
C. Bönnemann,
A. Foley,
P. Mohassel,
2018,
Matrix Biology.
Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium.
T. Irving,
L. Medne,
C. Ottenheijm,
2021,
The Journal of clinical investigation.
C. Bönnemann,
T. Lehky,
H. Lochmüller,
2020,
American journal of medical genetics. Part A.
R. Finkel,
C. Bönnemann,
P. Mohassel,
2017
.
M. Lek,
C. Bönnemann,
M. Deardorff,
2017,
Human molecular genetics.
A. Foley,
A. Kaindl,
D. Saade,
2022,
Neurology.
R. Finkel,
N. Staff,
L. Medne,
2019,
Annals of clinical and translational neurology.
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Beryl B. Cummings,
Carol J. Saunders,
C. Saunders,
2019,
Acta Neuropathologica.
M. Main,
C. Bönnemann,
L. Hynan,
2019,
Neurology.
Michael Bamshad,
Gabrielle Kardon,
Anne M. Moon,
2016,
Disease Models & Mechanisms.
Sita D Gupta,
K. Gable,
T. Dunn,
2022,
Neuropathology and applied neurobiology.
A. Mammen,
C. Bönnemann,
B. Schoser,
2022,
Journal of neuromuscular diseases.
A. Mammen,
C. Bönnemann,
S. Donkervoort,
2017,
Muscle & nerve.
A. Mammen,
L. Casciola-Rosen,
P. Mohassel,
2015,
Arthritis & rheumatology.
T. Roberts,
C. Bönnemann,
D. Rifkin,
2023,
bioRxiv.
P. Mohassel,
A. R. Foley,
Carsten G. Bönnemann,
2018,
Matrix biology : journal of the International Society for Matrix Biology.
Sita D Gupta,
Lucy Feng,
P. Mohassel,
2023,
Journal of neurology, neurosurgery, and psychiatry.
A. Arai,
L. Medne,
C. Bönnemann,
2023,
Annals of clinical and translational neurology.
Janelle Geist Hauserman,
Ying Hu,
P. Mohassel,
2024,
HGG advances.
T. Siddique,
S. Coppens,
P. Handford,
2021,
American journal of human genetics.