Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Durst, Ronen
Colombo, Roberto
Shpitzen, Shoshi
Avi, Liat Ben
Friedlander, Yechiel
Wexler, Roni
Raal, Frederick J.
Marais, David A.
Defesche, Joep C.
Mandelshtam, Michail Y.
Kotze, Maritha J.
Leitersdorf, Eran
and
Meiner, Vardiella
2001.
Recent Origin and Spread of a Common Lithuanian Mutation, G197del LDLR, Causing Familial Hypercholesterolemia: Positive Selection Is Not Always Necessary to Account for Disease Incidence among Ashkenazi Jews.
The American Journal of Human Genetics,
Vol. 68,
Issue. 5,
p.
1172.
Misbahuddin, Anjum
and
Warner, Thomas T.
2001.
Dystonia: an update on genetics and treatment.
Current Opinion in Neurology,
Vol. 14,
Issue. 4,
p.
471.
Gilbert, F.
2001.
Chromosome 9.
Genetic Testing,
Vol. 5,
Issue. 2,
p.
157.
Opal, Puneet
Tintner, Ron
Jankovic, Joseph
Leung, Joanne
Breakefield, Xandra O.
Friedman, Jennifer
and
Ozelius, Laurie
2002.
Intrafamilial phenotypic variability of the DYT1 dystonia: From asymptomatic TOR1A gene carrier status to dystonic storm.
Movement Disorders,
Vol. 17,
Issue. 2,
p.
339.
Gatto, Emilia Mabel
Pardal, Manuel Marı́a Fernandez
and
Micheli, Federico Eduardo
2003.
Unusual phenotypic expression of the DYT1 mutation.
Parkinsonism & Related Disorders,
Vol. 9,
Issue. 5,
p.
277.
Walker, Ruth H.
and
Shashidharan, P.
2003.
Developments in the molecular biology of DYT1 dystonia.
Movement Disorders,
Vol. 18,
Issue. 10,
p.
1102.
Carmona, J
Burguera, JA
Mollà, B
Mulas, F
Smeyers, P
Carratalà, F
De Yebenes, JG
Hoenicka, J
and
Palau, F
2003.
Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families.
Clinical Genetics,
Vol. 64,
Issue. 2,
p.
153.
Rechitsky, S
Verlinsky, O
Kuliev, A
Ozen, S
Laziuk, K
Beck, R
Gleicher, N
and
Verlinsky, Y
2004.
Preimplantation genetic diagnosis for early-onset torsion dystonia.
Reproductive BioMedicine Online,
Vol. 8,
Issue. 2,
p.
224.
Oriá, Reinaldo B
Patrick, Peter D
Zhang, Hong
Lorntz, Breyette
de Castro Costa, Carlos Maurício
Brito, Gerly A C
Barrett, Leah J
Lima, Aldo A M
and
Guerrant, Richard L
2005.
APOE4 Protects the Cognitive Development in Children with Heavy Diarrhea Burdens in Northeast Brazil.
Pediatric Research,
Vol. 57,
Issue. 2,
p.
310.
2005.
Practical Preimplantation Genetic Diagnosis.
p.
29.
Lin, Yen-Wen
Chang, Hsiu-Chen
Chou, Yah-Huei Wu
Chen, Rou-Shayn
Hsu, Wen-Chi
Wu, Wen-Shiang
Weng, Yi-Hsin
and
Lu, Chin-Song
2006.
DYT1 mutation in a cohort of Taiwanese primary dystonias.
Parkinsonism & Related Disorders,
Vol. 12,
Issue. 1,
p.
15.
Kamm, Christoph
Ozelius, Laurie J
and
Breakefield, Xandra O
2007.
TorsinA and
DYT1
early-onset dystonia
.
Future Neurology,
Vol. 3,
Issue. 1,
p.
61.
Fahn, Stanley
Jankovic, Joseph
Hallett, Mark
and
Jenner, Peter
2007.
Principles and Practice of Movement Disorders.
p.
307.
Frédéric, M. Y.
Clot, F.
Cif, L.
Blanchard, A.
Dürr, A.
Vuillaume, I.
Lesca, G.
Kreisler, A.
Davin, C.
Besnard, T.
Rousset, F.
Thorel, D.
Saquet, C.
Mechin, D.
Ozelius, L.
Agid, Y.
Barroso, B.
Chabrol, B.
Chan, V.
Clanet, M.
Coubes, C.
Destee, A.
Nguyen, K.
Vial, C.
Vidailhet, M.
Xie, J.
Sablonniere, B.
Calender, A.
Brice, A.
Roubertie, A.
Coubes, P.
Claustres, M.
Tuffery-Giraud, S.
and
Collod-Beroud, G.
2008.
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?.
Neurogenetics,
Vol. 9,
Issue. 2,
p.
143.
O'Roak, B J
Morgan, T M
Fishman, D O
Saus, E
Alonso, P
Gratacòs, M
Estivill, X
Teltsh, O
Kohn, Y
Kidd, K K
Cho, J
Lifton, R P
and
State, M W
2010.
Additional support for the association of SLITRK1 var321 and Tourette syndrome.
Molecular Psychiatry,
Vol. 15,
Issue. 5,
p.
447.
Fahn, Stanley
Jankovic, Joseph
and
Hallett, Mark
2011.
Principles and Practice of Movement Disorders.
p.
259.
Elia, Antonio E.
and
Albanese, Alberto
2011.
Hyperkinetic Movement Disorders.
p.
113.
Kuliev, Anver
2012.
Practical Preimplantation Genetic Diagnosis.
p.
45.
Cascalho, Ana
Jacquemyn, Julie
and
Goodchild, Rose E.
2017.
Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?.
Movement Disorders,
Vol. 32,
Issue. 3,
p.
371.
Kuliev, Anver
Rechitsky, Svetlana
and
Simpson, Joe Leigh
2020.
Practical Preimplantation Genetic Testing.
p.
49.