|1.||Breakefield, Xandra O: 9 articles (09/2010 - 02/2003)|
|2.||Hewett, Jeffrey W: 5 articles (09/2010 - 02/2003)|
|3.||Caldwell, Guy A: 3 articles (09/2010 - 04/2005)|
|4.||Caldwell, Kim A: 3 articles (09/2010 - 04/2005)|
|5.||Burdette, Alexander J: 2 articles (09/2010 - 09/2010)|
|6.||Balcioglu, Aygul: 2 articles (04/2010 - 08/2007)|
|7.||Sharma, Nutan: 2 articles (04/2010 - 08/2007)|
|8.||Ozelius, Laurie J: 2 articles (05/2009 - 02/2003)|
|9.||Nery, Flávia C: 2 articles (10/2008 - 05/2008)|
|10.||Zeng, Juan: 2 articles (10/2008 - 04/2006)|
|1.||Movement Disorders (Movement Disorder)
09/01/2015 - "Early-onset torsion dystonia (DYT1) is an autosomal-dominant movement disorder characterized by sustained muscle contractions and abnormal posturing. "
10/15/2008 - "A specific mutation (DeltaE) in torsinA underlies most cases of the dominantly inherited movement disorder, early-onset torsion dystonia (DYT1). "
05/01/2008 - "Early onset torsion dystonia are rare movement disorders. "
04/01/2006 - "Early onset torsion dystonia is a movement disorder inherited as an autosomal dominant syndrome with reduced penetrance. "
01/01/2006 - "Early onset torsion dystonia (EOTD) is a rare movement disorder characterized by involuntary, repetitive, sustained muscle contractions or postures involving one or more sites of the body. "
|2.||Dystonia (Limb Dystonia)
05/01/2009 - "DYT6 is a primary, early-onset torsion dystonia; however, unlike in DYT1 dystonia, the symptoms of DYT6 dystonia frequently involve the craniocervical region. "
11/01/2008 - "DYTI dystonia (DYT1-D, early-onset torsion dystonia) is caused by a GAG deletion in the DYTI gene. "
01/01/2008 - "DYT1 dystonia is a primary generalized early-onset torsion dystonia caused by mutations in DYT1 that codes for torsinA and has an autosomal dominant inheritance pattern with approximately 30% penetrance. "
01/01/2006 - "Early onset torsion dystonia (Oppenheim's dystonia)."
05/01/1998 - "Early-onset torsion dystonia, an autosomal dominant disease associated with the DYT1 locus on 9q34, is the most frequent genetic form of dystonia. "
|3.||Dystonic Disorders (Writer's Cramp)
04/01/2010 - "Early onset torsion dystonia (DYT1), the most common form of hereditary primary dystonia, is caused by a mutation in the TOR1A gene, which codes for the protein, torsinA. "
08/01/2007 - "Early onset torsion dystonia, the most common form of hereditary primary dystonia, is caused by a mutation in the TOR1A gene, which codes for the protein torsinA. "
12/01/1998 - "Both the discovery of the DYT1 gene on chromosome 9q34 in autosomal dominant early-onset torsion dystonia and the detection of linkage for one form of adult-onset focal dystonia to chromosome 18p (DYT7) in a family from northern Germany provide the opportunity to further investigate genetic factors in the focal dystonias. "
01/01/2012 - "DYT1, a primary dystonia, is well known as early-onset torsion dystonia with dominantly inherited generalized dystonia caused by a GAG deletion in the TOR1A gene located at 9q34.11. "
11/01/2008 - "[Case of DYT1 dystonia (early-onset torsion dystonia) showing long-term focal dystonia in the arm]."
09/08/2000 - "Early-onset torsion dystonia is an autosomal dominant hyperkinetic movement disorder that has recently been linked to a 3-base pair deletion in the DYT1 gene. "
12/13/2001 - "Early-onset torsion dystonia is a hyperkinetic movement disorder caused by a deletion of one glutamic acid residue in torsinA, a novel member of the AAA-family of ATPases. "
06/01/2001 - "Early-onset torsion dystonia is a hyperkinetic movement disorder caused by a deletion of 1 glutamic acid residue in torsin A protein, a novel member of the AAA family of adenosine triphosphatases. "
|1.||Glutamic Acid (Glutamate)
|2.||Adenosine Triphosphatases (ATPase)
|4.||Molecular Chaperones (Chaperone, Molecular)
|5.||Staphylococcal Protein A (A, Protein)
|6.||Proteins (Proteins, Gene)
|7.||Prostaglandins D (PGD)
|9.||DNA (Deoxyribonucleic Acid)