These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Reaching and writing movements: sensitive and reliable tools to measure genetic dystonia in children. Casellato C; Zorzi G; Pedrocchi A; Ferrigno G; Nardocci N J Child Neurol; 2011 Jul; 26(7):822-9. PubMed ID: 21421904 [TBL] [Abstract][Full Text] [Related]
24. Torsion dystonia in Israel. Korczyn AD; Kahana E; Zilber N; Streifler M; Carasso R; Alter M Ann Neurol; 1980 Oct; 8(4):387-91. PubMed ID: 7436383 [TBL] [Abstract][Full Text] [Related]
25. DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia. Groen JL; Ritz K; Warner TT; Baas F; Tijssen MA Parkinsonism Relat Disord; 2014 Jul; 20(7):782-5. PubMed ID: 24768614 [TBL] [Abstract][Full Text] [Related]
26. Pyridoxine for levodopa-induced dystonia. Jameson HD JAMA; 1970 Mar; 211(10):1700. PubMed ID: 5467095 [No Abstract] [Full Text] [Related]
27. Superior intelligence in sighted retinoblastoma patients and their families. Eldridge R; O'Meara K; Kitchin D J Med Genet; 1972 Sep; 9(3):331-5. PubMed ID: 5079105 [No Abstract] [Full Text] [Related]
28. Dystonia in Spain: study of a Gypsy family and general survey. Giménez-Roldán S; López-Fraile IP; Esteban A Adv Neurol; 1976; 14():125-36. PubMed ID: 941766 [TBL] [Abstract][Full Text] [Related]
34. A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia. Kousseff BG; Nichols P Birth Defects Orig Artic Ser; 1985; 21(2):111-7. PubMed ID: 4041573 [No Abstract] [Full Text] [Related]
35. Chromosomes in the de Lange syndrome. Sachdeva S; Smith GF Lancet; 1973 Apr; 1(7807):829. PubMed ID: 4121247 [No Abstract] [Full Text] [Related]
36. [Two cases of dystonia of motion of the lower limbs]. AMICI R Minerva Med; 1952 Apr; 43(29):754-5. PubMed ID: 14956783 [No Abstract] [Full Text] [Related]
37. Hereditary non-progressive torsion dystonia with intellectual disturbance. Nakashima K; Shimoda M; Sato K; Nanba E; Igo M; Sato K; Takahashi K Intern Med; 1995 Sep; 34(9):843-6. PubMed ID: 8580554 [TBL] [Abstract][Full Text] [Related]
38. Movement disorders in 2014. Genetic advances spark a revolution in dystonia phenotyping. de Koning TJ; Tijssen MA Nat Rev Neurol; 2015 Feb; 11(2):78-9. PubMed ID: 25561273 [TBL] [Abstract][Full Text] [Related]
39. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1621-4. PubMed ID: 7324662 [TBL] [Abstract][Full Text] [Related]
40. A genetic study of torsion dystonia. Bundey S; Harrison MJ; Marsden CD J Med Genet; 1975 Mar; 12(1):12-9. PubMed ID: 1121020 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]