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Showing 1 to 12 of 18 entries
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Hereditary paralysis agitans.

Ugeskrift for laeger

HOVE H.
PMID: 13169376
Ugeskr Laeger. 1954 Apr 22;116(16):614-6.

No abstract available.

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HOVE H. Paralysis agitans heriditaria. Hereditary paralysis agitans. Ugeskr Laeger. 1954;116(16):614-6
HOVE, H. (1954). Paralysis agitans heriditaria. Hereditary paralysis agitans. Ugeskrift for laeger, 116(16), 614-6.
HOVE, H. "Paralysis agitans heriditaria." Hereditary paralysis agitans. Ugeskrift for laeger vol. 116,16 (1954): 614-6.
HOVE H. Paralysis agitans heriditaria. Hereditary paralysis agitans. Ugeskr Laeger. 1954 Apr 22;116(16):614-6. Danish. PMID: 13169376.
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[New contribution on the heredity of parkinsonism].

Rivista di patologia nervosa e mentale

PINTUS G, SARTESCHI P.
PMID: 13101531
Riv Patol Nerv Ment. 1953;74(1):150-4.

No abstract available.

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PINTUS G, SARTESCHI P. Nuovo contributo all'ereditarietà del morbo di Parkinson. [New contribution on the heredity of parkinsonism]. Riv Patol Nerv Ment. 1953;74(1):150-4
PINTUS, G., & SARTESCHI, P. (1953). Nuovo contributo all'ereditarietà del morbo di Parkinson. [New contribution on the heredity of parkinsonism]. Rivista di patologia nervosa e mentale, 74(1), 150-4.
PINTUS, G, and SARTESCHI, P. "Nuovo contributo all'ereditarietà del morbo di Parkinson." [New contribution on the heredity of parkinsonism]. Rivista di patologia nervosa e mentale vol. 74,1 (1953): 150-4.
PINTUS G, SARTESCHI P. Nuovo contributo all'ereditarietà del morbo di Parkinson. [New contribution on the heredity of parkinsonism]. Riv Patol Nerv Ment. 1953;74(1):150-4. Undetermined. PMID: 13101531.
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[4 cases of familial juvenile paralysis agitans].

No to shinkei = Brain and nerve

NAGAO T, SHIKIBA S, IMAMURA M.
PMID: 13727410
No To Shinkei. 1961 Mar;13:201-4.

No abstract available.

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NAGAO T, SHIKIBA S, IMAMURA M. [4 cases of familial juvenile paralysis agitans]. No To Shinkei. 1961;13:201-4
NAGAO, T., SHIKIBA, S., & IMAMURA, M. (1961). [4 cases of familial juvenile paralysis agitans]. No to shinkei = Brain and nerve, 13201-4.
NAGAO, T, et al. "[4 cases of familial juvenile paralysis agitans]." No to shinkei = Brain and nerve vol. 13 (1961): 201-4.
NAGAO T, SHIKIBA S, IMAMURA M. [4 cases of familial juvenile paralysis agitans]. No To Shinkei. 1961 Mar;13:201-4. Japanese. PMID: 13727410.
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Reply: To PMID 25631192.

Annals of neurology

Tell-Martí G, Puig-Butille JA, Potrony M, Badenas C, Milà M, Malvehy J, Martí MJ, Ezquerra M, Fernández-Santiago R, Puig S.
PMID: 25913870
Ann Neurol. 2015 Jul;78(1):153-4. doi: 10.1002/ana.24418. Epub 2015 May 25.

No abstract available.

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Tell-Martí G, Puig-Butille JA, Potrony M, et al. Reply: To PMID 25631192. Ann Neurol. 2015;78(1):153-4doi: 10.1002/ana.24418.
Tell-Martí, G., Puig-Butille, J. A., Potrony, M., Badenas, C., Milà, M., Malvehy, J., Martí, M. J., Ezquerra, M., Fernández-Santiago, R., & Puig, S. (2015). Reply: To PMID 25631192. Annals of neurology, 78(1), 153-4. https://doi.org/10.1002/ana.24418
Tell-Martí, Gemma, et al. "Reply: To PMID 25631192." Annals of neurology vol. 78,1 (2015): 153-4. doi: https://doi.org/10.1002/ana.24418
Tell-Martí G, Puig-Butille JA, Potrony M, Badenas C, Milà M, Malvehy J, Martí MJ, Ezquerra M, Fernández-Santiago R, Puig S. Reply: To PMID 25631192. Ann Neurol. 2015 Jul;78(1):153-4. doi: 10.1002/ana.24418. Epub 2015 May 25. PMID: 25913870.
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Is the MC1R variant p.R160W associated with Parkinson's?.

Annals of neurology

Lubbe SJ, Escott-Price V, Brice A, Gasser T, Hardy J, Heutink P, Sharma M, Wood NW, Nalls M, Singleton AB, Williams NM, Morris HR.
PMID: 26389967
Ann Neurol. 2016 Jan;79(1):159-61. doi: 10.1002/ana.24527. Epub 2015 Dec 12.

No abstract available.

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Lubbe SJ, Escott-Price V, Brice A, et al. Is the MC1R variant p.R160W associated with Parkinson's?. Ann Neurol. 2015;79(1):159-61doi: 10.1002/ana.24527.
Lubbe, S. J., Escott-Price, V., Brice, A., Gasser, T., Hardy, J., Heutink, P., Sharma, M., Wood, N. W., Nalls, M., Singleton, A. B., Williams, N. M., Morris, H. R. (2016). Is the MC1R variant p.R160W associated with Parkinson's?. Annals of neurology, 79(1), 159-61. https://doi.org/10.1002/ana.24527
Lubbe, Steven J, et al. "Is the MC1R variant p.R160W associated with Parkinson's?." Annals of neurology vol. 79,1 (2016): 159-61. doi: https://doi.org/10.1002/ana.24527
Lubbe SJ, Escott-Price V, Brice A, Gasser T, Hardy J, Heutink P, Sharma M, Wood NW, Nalls M, Singleton AB, Williams NM, Morris HR. Is the MC1R variant p.R160W associated with Parkinson's?. Ann Neurol. 2016 Jan;79(1):159-61. doi: 10.1002/ana.24527. Epub 2015 Dec 12. PMID: 26389967; PMCID: PMC4738170.
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Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases.

Annals of neurology

Foo JN, Zhao Y, Liu J, Tan EK.
PMID: 25894970
Ann Neurol. 2015 Jul;78(1):152-3. doi: 10.1002/ana.24419. Epub 2015 May 25.

No abstract available.

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Foo JN, Zhao Y, Liu J, et al. Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases. Ann Neurol. 2015;78(1):152-3doi: 10.1002/ana.24419.
Foo, J. N., Zhao, Y., Liu, J., & Tan, E. K. (2015). Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases. Annals of neurology, 78(1), 152-3. https://doi.org/10.1002/ana.24419
Foo, Jia Nee, et al. "Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases." Annals of neurology vol. 78,1 (2015): 152-3. doi: https://doi.org/10.1002/ana.24419
Foo JN, Zhao Y, Liu J, Tan EK. Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases. Ann Neurol. 2015 Jul;78(1):152-3. doi: 10.1002/ana.24419. Epub 2015 May 25. PMID: 25894970.
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Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

PLoS genetics

Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N.
PMID: 21738487
PLoS Genet. 2011 Jun;7(6):e1002141. doi: 10.1371/journal.pgen.1002141. Epub 2011 Jun 23.

Although the causes of Parkinson's disease (PD) are thought to be primarily environmental, recent studies suggest that a number of genes influence susceptibility. Using targeted case recruitment and online survey instruments, we conducted the largest case-control genome-wide association study...

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Do CB, Tung JY, Dorfman E, et al. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet. 2011;7(6):e1002141doi: 10.1371/journal.pgen.1002141.
Do, C. B., Tung, J. Y., Dorfman, E., Kiefer, A. K., Drabant, E. M., Francke, U., Mountain, J. L., Goldman, S. M., Tanner, C. M., Langston, J. W., Wojcicki, A., & Eriksson, N. (2011). Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS genetics, 7(6), e1002141. https://doi.org/10.1371/journal.pgen.1002141
Do, Chuong B, et al. "Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease." PLoS genetics vol. 7,6 (2011): e1002141. doi: https://doi.org/10.1371/journal.pgen.1002141
Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet. 2011 Jun;7(6):e1002141. doi: 10.1371/journal.pgen.1002141. Epub 2011 Jun 23. PMID: 21738487; PMCID: PMC3121750.
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[Hereditary Parkinson disease. The Danish Society of Movement Disorders].

Ugeskrift for laeger

Hjermind LE, Nielsen JE.
PMID: 18397634
Ugeskr Laeger. 2008 Mar 17;170(12):1016.

No abstract available.

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Hjermind LE, Nielsen JE. Arvelig Parkinsons sygdom. Dansk Selskab for Bevaegeforstyrrelser. [Hereditary Parkinson disease. The Danish Society of Movement Disorders]. Ugeskr Laeger. 2008;170(12):1016
Hjermind, L. E., Nielsen, J. E. (2008). Arvelig Parkinsons sygdom. Dansk Selskab for Bevaegeforstyrrelser. [Hereditary Parkinson disease. The Danish Society of Movement Disorders]. Ugeskrift for laeger, 170(12), 1016.
Hjermind, Lena E, et al. "Arvelig Parkinsons sygdom. Dansk Selskab for Bevaegeforstyrrelser." [Hereditary Parkinson disease. The Danish Society of Movement Disorders]. Ugeskrift for laeger vol. 170,12 (2008): 1016.
Hjermind LE, Nielsen JE. Arvelig Parkinsons sygdom. Dansk Selskab for Bevaegeforstyrrelser. [Hereditary Parkinson disease. The Danish Society of Movement Disorders]. Ugeskr Laeger. 2008 Mar 17;170(12):1016. Danish. PMID: 18397634.
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The scientific and clinical basis for the treatment of Parkinson disease (2009).

Neurology

Olanow CW, Stern MB, Sethi K.
PMID: 19470958
Neurology. 2009 May 26;72(21):S1-136. doi: 10.1212/WNL.0b013e3181a1d44c.

Parkinson disease (PD) is an age-related neurodegenerative disorder that affects as many as 1-2% of persons aged 60 years and older. With the aging of the population, the frequency of PD is expected to increase dramatically in the coming...

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Olanow CW, Stern MB, Sethi K. The scientific and clinical basis for the treatment of Parkinson disease (2009). Neurology. 2009;72(21):S1-136doi: 10.1212/WNL.0b013e3181a1d44c.
Olanow, C. W., Stern, M. B., & Sethi, K. (2009). The scientific and clinical basis for the treatment of Parkinson disease (2009). Neurology, 72(21), S1-136. https://doi.org/10.1212/WNL.0b013e3181a1d44c
Olanow, C Warren, et al. "The scientific and clinical basis for the treatment of Parkinson disease (2009)." Neurology vol. 72,21 (2009): S1-136. doi: https://doi.org/10.1212/WNL.0b013e3181a1d44c
Olanow CW, Stern MB, Sethi K. The scientific and clinical basis for the treatment of Parkinson disease (2009). Neurology. 2009 May 26;72(21):S1-136. doi: 10.1212/WNL.0b013e3181a1d44c. PMID: 19470958.
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Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies.

Neurology

Pastor P.
PMID: 22786592
Neurology. 2012 Aug 14;79(7):619-20. doi: 10.1212/WNL.0b013e318264e3d2. Epub 2012 Jul 11.

No abstract available.

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Pastor P. Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies. Neurology. 2012;79(7):619-20doi: 10.1212/WNL.0b013e318264e3d2.
Pastor, P. (2012). Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies. Neurology, 79(7), 619-20. https://doi.org/10.1212/WNL.0b013e318264e3d2
Pastor, Pau. "Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies." Neurology vol. 79,7 (2012): 619-20. doi: https://doi.org/10.1212/WNL.0b013e318264e3d2
Pastor P. Genetic heterogeneity in Parkinson disease: the meaning of GWAS and replication studies. Neurology. 2012 Aug 14;79(7):619-20. doi: 10.1212/WNL.0b013e318264e3d2. Epub 2012 Jul 11. PMID: 22786592.
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Revisiting the relationship between essential tremor and Parkinson's disease.

Movement disorders : official journal of the Movement Disorder Society

Fekete R, Jankovic J.
PMID: 21462256
Mov Disord. 2011 Feb 15;26(3):391-8. doi: 10.1002/mds.23512.

BACKGROUND: The relationship between essential tremor and Parkinson's disease has been a subject of reviews and debates for long time, but there is now growing evidence that the two common movement disorders are pathogenically related, at least in some...

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Fekete R, Jankovic J. Revisiting the relationship between essential tremor and Parkinson's disease. Mov Disord. 2011;26(3):391-8doi: 10.1002/mds.23512.
Fekete, R., & Jankovic, J. (2011). Revisiting the relationship between essential tremor and Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, 26(3), 391-8. https://doi.org/10.1002/mds.23512
Fekete, R, and Jankovic, J. "Revisiting the relationship between essential tremor and Parkinson's disease." Movement disorders : official journal of the Movement Disorder Society vol. 26,3 (2011): 391-8. doi: https://doi.org/10.1002/mds.23512
Fekete R, Jankovic J. Revisiting the relationship between essential tremor and Parkinson's disease. Mov Disord. 2011 Feb 15;26(3):391-8. doi: 10.1002/mds.23512. PMID: 21462256.
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Using global team science to identify genetic parkinson's disease worldwide.

Annals of neurology

Vollstedt EJ, Kasten M, Klein C.
PMID: 31155756
Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26.

No abstract available.

Cite
Vollstedt EJ, Kasten M, Klein C. Using global team science to identify genetic parkinson's disease worldwide. Ann Neurol. 2019;86(2):153-157doi: 10.1002/ana.25514.
Vollstedt, E. J., Kasten, M., Klein, C. (2019). Using global team science to identify genetic parkinson's disease worldwide. Annals of neurology, 86(2), 153-157. https://doi.org/10.1002/ana.25514
Vollstedt, Eva-Juliane, et al. "Using global team science to identify genetic parkinson's disease worldwide." Annals of neurology vol. 86,2 (2019): 153-157. doi: https://doi.org/10.1002/ana.25514
Vollstedt EJ, Kasten M, Klein C. Using global team science to identify genetic parkinson's disease worldwide. Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26. PMID: 31155756; PMCID: PMC7410260.
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Showing 1 to 12 of 18 entries