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[Coronary computed tomography angiography for acute thoracic pain].

Medizinische Klinik, Intensivmedizin und Notfallmedizin

Haring B, von Ballmoos MW.
PMID: 23740108
Med Klin Intensivmed Notfmed. 2013 Jun;108(5):434-6. doi: 10.1007/s00063-013-0260-0. Epub 2013 Jun 07.

No abstract available.

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Haring B, von Ballmoos MW. Kardio-Computertomographie bei akutem Thoraxschmerz. [Coronary computed tomography angiography for acute thoracic pain]. Med Klin Intensivmed Notfmed. 2013;108(5):434-6doi: 10.1007/s00063-013-0260-0.
Haring, B., & von Ballmoos, M. W. (2013). Kardio-Computertomographie bei akutem Thoraxschmerz. [Coronary computed tomography angiography for acute thoracic pain]. Medizinische Klinik, Intensivmedizin und Notfallmedizin, 108(5), 434-6. https://doi.org/10.1007/s00063-013-0260-0
Haring, B, and von Ballmoos, M W. "Kardio-Computertomographie bei akutem Thoraxschmerz." [Coronary computed tomography angiography for acute thoracic pain]. Medizinische Klinik, Intensivmedizin und Notfallmedizin vol. 108,5 (2013): 434-6. doi: https://doi.org/10.1007/s00063-013-0260-0
Haring B, von Ballmoos MW. Kardio-Computertomographie bei akutem Thoraxschmerz. [Coronary computed tomography angiography for acute thoracic pain]. Med Klin Intensivmed Notfmed. 2013 Jun;108(5):434-6. doi: 10.1007/s00063-013-0260-0. Epub 2013 Jun 07. German. PMID: 23740108.
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Characterization of individual threading dislocations in GaN using ballistic electron emission microscopy.

Physical review letters

Im HJ, Ding Y, Pelz JP, Heying B, Speck JS.
PMID: 11531495
Phys Rev Lett. 2001 Sep 03;87(10):106802. doi: 10.1103/PhysRevLett.87.106802. Epub 2001 Aug 20.

Threading dislocations (TDs) of molecular beam epitaxy grown GaN film were studied with ultrahigh vacuum ballistic electron emission microscopy in order to quantify any fixed negative charge at identifiable TDs, with approximately 3 nm spatial and approximately 10 meV...

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Im HJ, Ding Y, Pelz JP, et al. Characterization of individual threading dislocations in GaN using ballistic electron emission microscopy. Phys Rev Lett. 2001;87(10):106802doi: 10.1103/PhysRevLett.87.106802.
Im, H. J., Ding, Y., Pelz, J. P., Heying, B., & Speck, J. S. (2001). Characterization of individual threading dislocations in GaN using ballistic electron emission microscopy. Physical review letters, 87(10), 106802. https://doi.org/10.1103/PhysRevLett.87.106802
Im, H J, et al. "Characterization of individual threading dislocations in GaN using ballistic electron emission microscopy." Physical review letters vol. 87,10 (2001): 106802. doi: https://doi.org/10.1103/PhysRevLett.87.106802
Im HJ, Ding Y, Pelz JP, Heying B, Speck JS. Characterization of individual threading dislocations in GaN using ballistic electron emission microscopy. Phys Rev Lett. 2001 Sep 03;87(10):106802. doi: 10.1103/PhysRevLett.87.106802. Epub 2001 Aug 20. PMID: 11531495.
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Transfer of salt tolerance from Aeleuropus littorulis sinensis to wheat (Triticum aestivum L.) via asymmetric somatic hybridization.

Plant science : an international journal of experimental plant biology

Wei Y, Guangmin X, Daying Z, Huimin C.
PMID: 11448756
Plant Sci. 2001 Jul;161(2):259-266. doi: 10.1016/s0168-9452(01)00382-x.

Protoplasts of wheat c.v. Jinan 177 were fused by PEG method with the UV irradiated protoplasts of A. littoralis - a salt tolerant plant intertribal to wheat. The early-formed regenerated clones were identified as hybrids by chromosome, isozyme and...

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Wei Y, Guangmin X, Daying Z, et al. Transfer of salt tolerance from Aeleuropus littorulis sinensis to wheat (Triticum aestivum L.) via asymmetric somatic hybridization. Plant Sci. 2001;161(2):259-266doi: 10.1016/s0168-9452(01)00382-x.
Wei, Y., Guangmin, X., Daying, Z., & Huimin, C. (2001). Transfer of salt tolerance from Aeleuropus littorulis sinensis to wheat (Triticum aestivum L.) via asymmetric somatic hybridization. Plant science : an international journal of experimental plant biology, 161(2), 259-266. https://doi.org/10.1016/s0168-9452(01)00382-x
Wei, Y, et al. "Transfer of salt tolerance from Aeleuropus littorulis sinensis to wheat (Triticum aestivum L.) via asymmetric somatic hybridization." Plant science : an international journal of experimental plant biology vol. 161,2 (2001): 259-266. doi: https://doi.org/10.1016/s0168-9452(01)00382-x
Wei Y, Guangmin X, Daying Z, Huimin C. Transfer of salt tolerance from Aeleuropus littorulis sinensis to wheat (Triticum aestivum L.) via asymmetric somatic hybridization. Plant Sci. 2001 Jul;161(2):259-266. doi: 10.1016/s0168-9452(01)00382-x. PMID: 11448756.
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Linkage Data for Group IV Markers in Neurospora.

Genetics

Maling B.
PMID: 17247887
Genetics. 1959 Nov;44(6):1215-20. doi: 10.1093/genetics/44.6.1215.

No abstract available.

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Maling B. Linkage Data for Group IV Markers in Neurospora. Genetics. 1959;44(6):1215-20doi: 10.1093/genetics/44.6.1215.
Maling, B. (1959). Linkage Data for Group IV Markers in Neurospora. Genetics, 44(6), 1215-20. https://doi.org/10.1093/genetics/44.6.1215
Maling, B. "Linkage Data for Group IV Markers in Neurospora." Genetics vol. 44,6 (1959): 1215-20. doi: https://doi.org/10.1093/genetics/44.6.1215
Maling B. Linkage Data for Group IV Markers in Neurospora. Genetics. 1959 Nov;44(6):1215-20. doi: 10.1093/genetics/44.6.1215. PMID: 17247887; PMCID: PMC1224427.
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Abnormal DaTSCAN and Atypical Parkinsonism in SCA12.

Movement disorders clinical practice

Latorre A, Del Gamba C, Menozzi E, Balint B, Brugger F, Bhatia KP.
PMID: 31286011
Mov Disord Clin Pract. 2019 Mar 28;6(5):400-402. doi: 10.1002/mdc3.12751. eCollection 2019 Jun.

No abstract available.

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Latorre A, Del Gamba C, Menozzi E, et al. Abnormal DaTSCAN and Atypical Parkinsonism in SCA12. Mov Disord Clin Pract. 2019;6(5):400-402doi: 10.1002/mdc3.12751.
Latorre, A., Del Gamba, C., Menozzi, E., Balint, B., Brugger, F., & Bhatia, K. P. (2019). Abnormal DaTSCAN and Atypical Parkinsonism in SCA12. Movement disorders clinical practice, 6(5), 400-402. https://doi.org/10.1002/mdc3.12751
Latorre, Anna, et al. "Abnormal DaTSCAN and Atypical Parkinsonism in SCA12." Movement disorders clinical practice vol. 6,5 (2019): 400-402. doi: https://doi.org/10.1002/mdc3.12751
Latorre A, Del Gamba C, Menozzi E, Balint B, Brugger F, Bhatia KP. Abnormal DaTSCAN and Atypical Parkinsonism in SCA12. Mov Disord Clin Pract. 2019 Mar 28;6(5):400-402. doi: 10.1002/mdc3.12751. eCollection 2019 Jun. PMID: 31286011; PMCID: PMC6592799.
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The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain Immunosurveillance.

Movement disorders clinical practice

Balint B, Stamelou M.
PMID: 30363541
Mov Disord Clin Pract. 2015 Nov 27;3(1):29-30. doi: 10.1002/mdc3.12282. eCollection 2016.

No abstract available.

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Balint B, Stamelou M. The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain Immunosurveillance. Mov Disord Clin Pract. 2015;3(1):29-30doi: 10.1002/mdc3.12282.
Balint, B., & Stamelou, M. (2016). The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain Immunosurveillance. Movement disorders clinical practice, 3(1), 29-30. https://doi.org/10.1002/mdc3.12282
Balint, Bettina, and Stamelou, Maria. "The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain Immunosurveillance." Movement disorders clinical practice vol. 3,1 (2016): 29-30. doi: https://doi.org/10.1002/mdc3.12282
Balint B, Stamelou M. The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain Immunosurveillance. Mov Disord Clin Pract. 2015 Nov 27;3(1):29-30. doi: 10.1002/mdc3.12282. eCollection 2016. PMID: 30363541; PMCID: PMC6178593.
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Pragmatic Treatment of Stiff Person Spectrum Disorders.

Movement disorders clinical practice

Balint B, Meinck HM.
PMID: 30363317
Mov Disord Clin Pract. 2018 Jul 19;5(4):394-401. doi: 10.1002/mdc3.12629. eCollection 2018.

BACKGROUND: Stiff person spectrum disorders (SPSD) are a group of rare conditions clinically characterized by stiffness, spasms, and heightened stimulus sensitivity. They also share a spectrum of antibodies.METHODS: We reviewed the literature and our own experience with the aim...

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Balint B, Meinck HM. Pragmatic Treatment of Stiff Person Spectrum Disorders. Mov Disord Clin Pract. 2018;5(4):394-401doi: 10.1002/mdc3.12629.
Balint, B., & Meinck, H. M. (2018). Pragmatic Treatment of Stiff Person Spectrum Disorders. Movement disorders clinical practice, 5(4), 394-401. https://doi.org/10.1002/mdc3.12629
Balint, Bettina, and Meinck, Hans-Michael. "Pragmatic Treatment of Stiff Person Spectrum Disorders." Movement disorders clinical practice vol. 5,4 (2018): 394-401. doi: https://doi.org/10.1002/mdc3.12629
Balint B, Meinck HM. Pragmatic Treatment of Stiff Person Spectrum Disorders. Mov Disord Clin Pract. 2018 Jul 19;5(4):394-401. doi: 10.1002/mdc3.12629. eCollection 2018. PMID: 30363317; PMCID: PMC6174384.
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Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome.

Movement disorders clinical practice

Balint B, Bhatia KP.
PMID: 30363511
Mov Disord Clin Pract. 2015 Jun 04;2(3):230-231. doi: 10.1002/mdc3.12178. eCollection 2015 Sep.

No abstract available.

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Balint B, Bhatia KP. Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome. Mov Disord Clin Pract. 2015;2(3):230-231doi: 10.1002/mdc3.12178.
Balint, B., & Bhatia, K. P. (2015). Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome. Movement disorders clinical practice, 2(3), 230-231. https://doi.org/10.1002/mdc3.12178
Balint, Bettina, and Bhatia, Kailash P. "Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome." Movement disorders clinical practice vol. 2,3 (2015): 230-231. doi: https://doi.org/10.1002/mdc3.12178
Balint B, Bhatia KP. Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome. Mov Disord Clin Pract. 2015 Jun 04;2(3):230-231. doi: 10.1002/mdc3.12178. eCollection 2015 Sep. PMID: 30363511; PMCID: PMC6178692.
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Expert comment to: Novel Xp21.1 deletion associated with unusual features in large McLeod syndrome kindred.

Parkinsonism & related disorders

Balint B, Lang AE.
PMID: 30858069
Parkinsonism Relat Disord. 2020 Oct;79:133-134. doi: 10.1016/j.parkreldis.2019.02.024. Epub 2019 Feb 19.

No abstract available.

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Balint B, Lang AE. Expert comment to: Novel Xp21.1 deletion associated with unusual features in large McLeod syndrome kindred. Parkinsonism Relat Disord. 2019;79:133-134doi: 10.1016/j.parkreldis.2019.02.024.
Balint, B., & Lang, A. E. (2020). Expert comment to: Novel Xp21.1 deletion associated with unusual features in large McLeod syndrome kindred. Parkinsonism & related disorders, 79133-134. https://doi.org/10.1016/j.parkreldis.2019.02.024
Balint, Bettina, and Lang, Anthony E. "Expert comment to: Novel Xp21.1 deletion associated with unusual features in large McLeod syndrome kindred." Parkinsonism & related disorders vol. 79 (2020): 133-134. doi: https://doi.org/10.1016/j.parkreldis.2019.02.024
Balint B, Lang AE. Expert comment to: Novel Xp21.1 deletion associated with unusual features in large McLeod syndrome kindred. Parkinsonism Relat Disord. 2020 Oct;79:133-134. doi: 10.1016/j.parkreldis.2019.02.024. Epub 2019 Feb 19. PMID: 30858069.
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Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes.

Movement disorders clinical practice

Erro R, Balint B, Kurian MA, Brugger F, Picillo M, Barone P, Bhatia KP, Pellecchia MT.
PMID: 30868093
Mov Disord Clin Pract. 2016 Mar 31;4(1):125-128. doi: 10.1002/mdc3.12319. eCollection 2017.

No abstract available.

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Erro R, Balint B, Kurian MA, et al. Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes. Mov Disord Clin Pract. 2016;4(1):125-128doi: 10.1002/mdc3.12319.
Erro, R., Balint, B., Kurian, M. A., Brugger, F., Picillo, M., Barone, P., Bhatia, K. P., & Pellecchia, M. T. (2017). Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes. Movement disorders clinical practice, 4(1), 125-128. https://doi.org/10.1002/mdc3.12319
Erro, Roberto, et al. "Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes." Movement disorders clinical practice vol. 4,1 (2017): 125-128. doi: https://doi.org/10.1002/mdc3.12319
Erro R, Balint B, Kurian MA, Brugger F, Picillo M, Barone P, Bhatia KP, Pellecchia MT. Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes. Mov Disord Clin Pract. 2016 Mar 31;4(1):125-128. doi: 10.1002/mdc3.12319. eCollection 2017. PMID: 30868093; PMCID: PMC6407056.
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Some New and Unexpected Tauopathies in Movement Disorders.

Movement disorders clinical practice

Mulroy E, Jaunmuktane Z, Balint B, Erro R, Latorre A, Bhatia KP.
PMID: 32775506
Mov Disord Clin Pract. 2020 Aug 03;7(6):616-626. doi: 10.1002/mdc3.12995. eCollection 2020 Aug.

No abstract available.

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Mulroy E, Jaunmuktane Z, Balint B, et al. Some New and Unexpected Tauopathies in Movement Disorders. Mov Disord Clin Pract. 2020;7(6):616-626doi: 10.1002/mdc3.12995.
Mulroy, E., Jaunmuktane, Z., Balint, B., Erro, R., Latorre, A., & Bhatia, K. P. (2020). Some New and Unexpected Tauopathies in Movement Disorders. Movement disorders clinical practice, 7(6), 616-626. https://doi.org/10.1002/mdc3.12995
Mulroy, Eoin, et al. "Some New and Unexpected Tauopathies in Movement Disorders." Movement disorders clinical practice vol. 7,6 (2020): 616-626. doi: https://doi.org/10.1002/mdc3.12995
Mulroy E, Jaunmuktane Z, Balint B, Erro R, Latorre A, Bhatia KP. Some New and Unexpected Tauopathies in Movement Disorders. Mov Disord Clin Pract. 2020 Aug 03;7(6):616-626. doi: 10.1002/mdc3.12995. eCollection 2020 Aug. PMID: 32775506; PMCID: PMC7396854.
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Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease.

Movement disorders clinical practice

Balint B, Stephen CD, Udani V, Sankhla CS, Barad NH, Lang AE, Bhatia KP.
PMID: 31061839
Mov Disord Clin Pract. 2019 Apr 04;6(4):312-315. doi: 10.1002/mdc3.12747. eCollection 2019 Apr.

METHODS: Case series of four patients with RESULTS: The patients displayed characteristic episodes of dystonic arm posturing, involving a dystonic, flexed arm held in front of the body or close to the body, but with the hand raised upwards....

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Balint B, Stephen CD, Udani V, et al. Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease. Mov Disord Clin Pract. 2019;6(4):312-315doi: 10.1002/mdc3.12747.
Balint, B., Stephen, C. D., Udani, V., Sankhla, C. S., Barad, N. H., Lang, A. E., & Bhatia, K. P. (2019). Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease. Movement disorders clinical practice, 6(4), 312-315. https://doi.org/10.1002/mdc3.12747
Balint, Bettina, et al. "Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease." Movement disorders clinical practice vol. 6,4 (2019): 312-315. doi: https://doi.org/10.1002/mdc3.12747
Balint B, Stephen CD, Udani V, Sankhla CS, Barad NH, Lang AE, Bhatia KP. Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease. Mov Disord Clin Pract. 2019 Apr 04;6(4):312-315. doi: 10.1002/mdc3.12747. eCollection 2019 Apr. PMID: 31061839; PMCID: PMC6476601.
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Showing 1 to 12 of 156 entries