Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 36 of 318 entries
Sorted by: Best Match Show Resources per page
Microbiology of Cardiac Implantable Electronic Device Infections.

JACC. Clinical electrophysiology

Hussein AA, Baghdy Y, Wazni OM, Brunner MP, Kabbach G, Shao M, Gordon S, Saliba WI, Wilkoff BL, Tarakji KG.
PMID: 29759872
JACC Clin Electrophysiol. 2016 Aug;2(4):498-505. doi: 10.1016/j.jacep.2016.01.019. Epub 2016 Apr 06.

OBJECTIVES: This study reports a high-volume tertiary care center experience with the microbiology of cardiac implantable electronic devices (CIED) infections with assessment of temporal trends and profiles of late versus early infections.BACKGROUND: The rates of CIED infections have been...

Cite
Hussein AA, Baghdy Y, Wazni OM, et al. Microbiology of Cardiac Implantable Electronic Device Infections. JACC Clin Electrophysiol. 2016;2(4):498-505doi: 10.1016/j.jacep.2016.01.019.
Hussein, A. A., Baghdy, Y., Wazni, O. M., Brunner, M. P., Kabbach, G., Shao, M., Gordon, S., Saliba, W. I., Wilkoff, B. L., & Tarakji, K. G. (2016). Microbiology of Cardiac Implantable Electronic Device Infections. JACC. Clinical electrophysiology, 2(4), 498-505. https://doi.org/10.1016/j.jacep.2016.01.019
Hussein, Ayman A, et al. "Microbiology of Cardiac Implantable Electronic Device Infections." JACC. Clinical electrophysiology vol. 2,4 (2016): 498-505. doi: https://doi.org/10.1016/j.jacep.2016.01.019
Hussein AA, Baghdy Y, Wazni OM, Brunner MP, Kabbach G, Shao M, Gordon S, Saliba WI, Wilkoff BL, Tarakji KG. Microbiology of Cardiac Implantable Electronic Device Infections. JACC Clin Electrophysiol. 2016 Aug;2(4):498-505. doi: 10.1016/j.jacep.2016.01.019. Epub 2016 Apr 06. PMID: 29759872.
Copy Download .nbib Format: NLM
A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies.

Frontiers in pediatrics

van de Putte R, Dworschak GC, Brosens E, Reutter HM, Marcelis CLM, Acuna-Hidalgo R, Kurtas NE, Steehouwer M, Dunwoodie SL, Schmiedeke E, Märzheuser S, Schwarzer N, Brooks AS, de Klein A, Sloots CEJ, Tibboel D, Brisighelli G, Morandi A, Bedeschi MF, Bates MD, Levitt MA, Peña A, de Blaauw I, Roeleveld N, Brunner HG, van Rooij IALM, Hoischen A.
PMID: 32656166
Front Pediatr. 2020 Jun 23;8:310. doi: 10.3389/fped.2020.00310. eCollection 2020.

No abstract available.

Cite
van de Putte R, Dworschak GC, Brosens E, et al. A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Front Pediatr. 2020;8:310doi: 10.3389/fped.2020.00310.
van de Putte, R., Dworschak, G. C., Brosens, E., Reutter, H. M., Marcelis, C. L. M., Acuna-Hidalgo, R., Kurtas, N. E., Steehouwer, M., Dunwoodie, S. L., Schmiedeke, E., Märzheuser, S., Schwarzer, N., Brooks, A. S., de Klein, A., Sloots, C. E. J., Tibboel, D., Brisighelli, G., Morandi, A., Bedeschi, M. F., Bates, M. D., Levitt, M. A., Peña, A., de Blaauw, I., Roeleveld, N., Brunner, H. G., van Rooij, I. A. L. M., & Hoischen, A. (2020). A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in pediatrics, 8310. https://doi.org/10.3389/fped.2020.00310
van de Putte, Romy, et al. "A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies." Frontiers in pediatrics vol. 8 (2020): 310. doi: https://doi.org/10.3389/fped.2020.00310
van de Putte R, Dworschak GC, Brosens E, Reutter HM, Marcelis CLM, Acuna-Hidalgo R, Kurtas NE, Steehouwer M, Dunwoodie SL, Schmiedeke E, Märzheuser S, Schwarzer N, Brooks AS, de Klein A, Sloots CEJ, Tibboel D, Brisighelli G, Morandi A, Bedeschi MF, Bates MD, Levitt MA, Peña A, de Blaauw I, Roeleveld N, Brunner HG, van Rooij IALM, Hoischen A. A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Front Pediatr. 2020 Jun 23;8:310. doi: 10.3389/fped.2020.00310. eCollection 2020. PMID: 32656166; PMCID: PMC7324789.
Copy Download .nbib Format: NLM
Trend-Analysis of Solid-State Structures: Low-Energy Conformational 'Reactions' Involving Directed and Coupled Movements in Half-Sandwich Compounds [CpFe(CO){C(=O)R}PPh.

ChemistryOpen

Brunner H, Tsuno T.
PMID: 29744281
ChemistryOpen. 2018 Apr 16;7(5):312. doi: 10.1002/open.201800042. eCollection 2018 May.

Invited for this month's cover picture are Prof. Dr. Henri Brunner from the University of Regensburg (Germany) and Prof. Dr. Takashi Tsuno from Nihon University (Japan). The cover picture shows the conformational reaction of JIDLUD→FIHTUL. The order of sample...

Cite
Brunner H, Tsuno T. Trend-Analysis of Solid-State Structures: Low-Energy Conformational 'Reactions' Involving Directed and Coupled Movements in Half-Sandwich Compounds [CpFe(CO){C(=O)R}PPh. ChemistryOpen. 2018;7(5):312doi: 10.1002/open.201800042.
Brunner, H., & Tsuno, T. (2018). Trend-Analysis of Solid-State Structures: Low-Energy Conformational 'Reactions' Involving Directed and Coupled Movements in Half-Sandwich Compounds [CpFe(CO){C(=O)R}PPh. ChemistryOpen, 7(5), 312. https://doi.org/10.1002/open.201800042
Brunner, Henri, and Tsuno, Takashi. "Trend-Analysis of Solid-State Structures: Low-Energy Conformational 'Reactions' Involving Directed and Coupled Movements in Half-Sandwich Compounds [CpFe(CO){C(=O)R}PPh." ChemistryOpen vol. 7,5 (2018): 312. doi: https://doi.org/10.1002/open.201800042
Brunner H, Tsuno T. Trend-Analysis of Solid-State Structures: Low-Energy Conformational 'Reactions' Involving Directed and Coupled Movements in Half-Sandwich Compounds [CpFe(CO){C(=O)R}PPh. ChemistryOpen. 2018 Apr 16;7(5):312. doi: 10.1002/open.201800042. eCollection 2018 May. PMID: 29744281; PMCID: PMC5931536.
Copy Download .nbib Format: NLM
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nature communications

Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM.
PMID: 31048695
Nat Commun. 2019 May 02;10(1):2079. doi: 10.1038/s41467-019-10161-9.

The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

Cite
Snijders Blok L, Rousseau J, Twist J, et al. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun. 2019;10(1):2079doi: 10.1038/s41467-019-10161-9.
Snijders Blok, L., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., Agbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Koopmans, M., Brilstra, E. H., Monroe, G. R., van Gassen, K. L. I., van Binsbergen, E., Newbury-Ecob, R., Bownass, L., Bader, I., Mayr, J. A., Wortmann, S. B., Jakielski, K. J., Strand, E. A., Kloth, K., Bierhals, T., Roberts, J. D., Petrovich, R. M., Machida, S., Kurumizaka, H., Lelieveld, S., Pfundt, R., Jansen, S., Deriziotis, P., Faivre, L., Thevenon, J., Assoum, M., Shriberg, L., Kleefstra, T., Brunner, H. G., Wade, P. A., Fisher, S. E., & Campeau, P. M. (2019). Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature communications, 10(1), 2079. https://doi.org/10.1038/s41467-019-10161-9
Snijders Blok, Lot, et al. "Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language." Nature communications vol. 10,1 (2019): 2079. doi: https://doi.org/10.1038/s41467-019-10161-9
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T, Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun. 2019 May 02;10(1):2079. doi: 10.1038/s41467-019-10161-9. PMID: 31048695; PMCID: PMC6497626.
Copy Download .nbib Format: NLM
Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons.

Neurobiology of disease

van Rhijn JR, Shi Y, Bormann M, Mossink B, Frega M, Recaioglu H, Hakobjan M, Klein Gunnewiek T, Schoenmaker C, Palmer E, Faivre L, Kittel-Schneider S, Schubert D, Brunner H, Franke B, Nadif Kasri N.
PMID: 34923109
Neurobiol Dis. 2021 Dec 16;163:105587. doi: 10.1016/j.nbd.2021.105587. Epub 2021 Dec 16.

Monoamine neurotransmitter abundance affects motor control, emotion, and cognitive function and is regulated by monoamine oxidases. Among these, Monoamine oxidase A (MAOA) catalyzes the degradation of dopamine, norepinephrine, and serotonin into their inactive metabolites. Loss-of-function mutations in the X-linked...

Cite
van Rhijn JR, Shi Y, Bormann M, et al. Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons. Neurobiol Dis. 2021;163:105587doi: 10.1016/j.nbd.2021.105587.
van Rhijn, J. R., Shi, Y., Bormann, M., Mossink, B., Frega, M., Recaioglu, H., Hakobjan, M., Klein Gunnewiek, T., Schoenmaker, C., Palmer, E., Faivre, L., Kittel-Schneider, S., Schubert, D., Brunner, H., Franke, B., & Nadif Kasri, N. (2021). Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons. Neurobiology of disease, 163105587. https://doi.org/10.1016/j.nbd.2021.105587
van Rhijn, Jon-Ruben, et al. "Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons." Neurobiology of disease vol. 163 (2021): 105587. doi: https://doi.org/10.1016/j.nbd.2021.105587
van Rhijn JR, Shi Y, Bormann M, Mossink B, Frega M, Recaioglu H, Hakobjan M, Klein Gunnewiek T, Schoenmaker C, Palmer E, Faivre L, Kittel-Schneider S, Schubert D, Brunner H, Franke B, Nadif Kasri N. Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons. Neurobiol Dis. 2021 Dec 16;163:105587. doi: 10.1016/j.nbd.2021.105587. Epub 2021 Dec 16. PMID: 34923109.
Copy Download .nbib Format: NLM
Comparison of human and rodent cell models to study myocardial lipid-induced insulin resistance.

Prostaglandins, leukotrienes, and essential fatty acids

Wong LY, Glatz JFC, Wang S, Geraets IME, Vanherle S, Wijngaard AVD, Brunner H, Luiken JJFP, Nabben M.
PMID: 33751940
Prostaglandins Leukot Essent Fatty Acids. 2021 Apr;167:102267. doi: 10.1016/j.plefa.2021.102267. Epub 2021 Mar 13.

Isolated or cultured cells have proven to be valuable model systems to investigate cellular (patho)biology and for screening of the efficacy of drugs or their possible side-effects. Pluripotent stem cells (PSC) can be readily obtained from healthy individuals as...

Cite
Wong LY, Glatz JFC, Wang S, et al. Comparison of human and rodent cell models to study myocardial lipid-induced insulin resistance. Prostaglandins Leukot Essent Fatty Acids. 2021;167:102267doi: 10.1016/j.plefa.2021.102267.
Wong, L. Y., Glatz, J. F. C., Wang, S., Geraets, I. M. E., Vanherle, S., Wijngaard, A. V. D., Brunner, H., Luiken, J. J. F. P., & Nabben, M. (2021). Comparison of human and rodent cell models to study myocardial lipid-induced insulin resistance. Prostaglandins, leukotrienes, and essential fatty acids, 167102267. https://doi.org/10.1016/j.plefa.2021.102267
Wong, Li-Yen, et al. "Comparison of human and rodent cell models to study myocardial lipid-induced insulin resistance." Prostaglandins, leukotrienes, and essential fatty acids vol. 167 (2021): 102267. doi: https://doi.org/10.1016/j.plefa.2021.102267
Wong LY, Glatz JFC, Wang S, Geraets IME, Vanherle S, Wijngaard AVD, Brunner H, Luiken JJFP, Nabben M. Comparison of human and rodent cell models to study myocardial lipid-induced insulin resistance. Prostaglandins Leukot Essent Fatty Acids. 2021 Apr;167:102267. doi: 10.1016/j.plefa.2021.102267. Epub 2021 Mar 13. PMID: 33751940.
Copy Download .nbib Format: NLM
Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis.

Rheumatology (Oxford, England)

Ruperto N, Brunner HI, Pacheco-Tena C, Louw I, Vega-Cornejo G, Spindler AJ, Kingsbury DJ, Schmeling H, Borzutzky A, Cuttica R, Inman CJ, Malievskiy V, Scott C, Keltsev V, Terreri MT, Viola DO, Xavier RM, Fernandes TAP, Velázquez MDRM, Henrickson M, Clark MB, Bensley KA, Li X, Lo KH, Leu JH, Hsu CH, Hsia EC, Xu Z, Martini A, Lovell DJ.
PMID: 33493312
Rheumatology (Oxford). 2021 Oct 02;60(10):4495-4507. doi: 10.1093/rheumatology/keab021.

OBJECTIVES: To assess efficacy, pharmacokinetics (PK) and safety of intravenous (i.v.) golimumab in patients with polyarticular-course JIA (pc-JIA).METHODS: Children aged 2 to

Cite
Ruperto N, Brunner HI, Pacheco-Tena C, et al. Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis. Rheumatology (Oxford). 2021;60(10):4495-4507doi: 10.1093/rheumatology/keab021.
Ruperto, N., Brunner, H. I., Pacheco-Tena, C., Louw, I., Vega-Cornejo, G., Spindler, A. J., Kingsbury, D. J., Schmeling, H., Borzutzky, A., Cuttica, R., Inman, C. J., Malievskiy, V., Scott, C., Keltsev, V., Terreri, M. T., Viola, D. O., Xavier, R. M., Fernandes, T. A. P., Velázquez, M. D. R. M., Henrickson, M., Clark, M. B., Bensley, K. A., Li, X., Lo, K. H., Leu, J. H., Hsu, C. H., Hsia, E. C., Xu, Z., Martini, A., Lovell, D. J. (2021). Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis. Rheumatology (Oxford, England), 60(10), 4495-4507. https://doi.org/10.1093/rheumatology/keab021
Ruperto, Nicolino, et al. "Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis." Rheumatology (Oxford, England) vol. 60,10 (2021): 4495-4507. doi: https://doi.org/10.1093/rheumatology/keab021
Ruperto N, Brunner HI, Pacheco-Tena C, Louw I, Vega-Cornejo G, Spindler AJ, Kingsbury DJ, Schmeling H, Borzutzky A, Cuttica R, Inman CJ, Malievskiy V, Scott C, Keltsev V, Terreri MT, Viola DO, Xavier RM, Fernandes TAP, Velázquez MDRM, Henrickson M, Clark MB, Bensley KA, Li X, Lo KH, Leu JH, Hsu CH, Hsia EC, Xu Z, Martini A, Lovell DJ. Open-label phase 3 study of intravenous golimumab in patients with polyarticular juvenile idiopathic arthritis. Rheumatology (Oxford). 2021 Oct 02;60(10):4495-4507. doi: 10.1093/rheumatology/keab021. PMID: 33493312; PMCID: PMC8487314.
Copy Download .nbib Format: NLM
Palliative care and coping in patients with acute myeloid leukemia: Mediation analysis of data from a randomized clinical trial.

Cancer

Nelson AM, Amonoo HL, Kavanaugh AR, Webb JA, Jackson VA, Rice J, Lavoie MW, Fathi AT, Brunner AM, Greer JA, Temel JS, El-Jawahri A, LeBlanc TW.
PMID: 34460937
Cancer. 2021 Dec 15;127(24):4702-4710. doi: 10.1002/cncr.33886. Epub 2021 Aug 30.

BACKGROUND: It has been shown previously that integrated palliative care for patients with acute myeloid leukemia (AML) during intensive chemotherapy leads to improvements in quality of life (QOL) and mood. Coping has been shown to mediate palliative care interventions...

Cite
Nelson AM, Amonoo HL, Kavanaugh AR, et al. Palliative care and coping in patients with acute myeloid leukemia: Mediation analysis of data from a randomized clinical trial. Cancer. 2021;127(24):4702-4710doi: 10.1002/cncr.33886.
Nelson, A. M., Amonoo, H. L., Kavanaugh, A. R., Webb, J. A., Jackson, V. A., Rice, J., Lavoie, M. W., Fathi, A. T., Brunner, A. M., Greer, J. A., Temel, J. S., El-Jawahri, A., & LeBlanc, T. W. (2021). Palliative care and coping in patients with acute myeloid leukemia: Mediation analysis of data from a randomized clinical trial. Cancer, 127(24), 4702-4710. https://doi.org/10.1002/cncr.33886
Nelson, Ashley M, et al. "Palliative care and coping in patients with acute myeloid leukemia: Mediation analysis of data from a randomized clinical trial." Cancer vol. 127,24 (2021): 4702-4710. doi: https://doi.org/10.1002/cncr.33886
Nelson AM, Amonoo HL, Kavanaugh AR, Webb JA, Jackson VA, Rice J, Lavoie MW, Fathi AT, Brunner AM, Greer JA, Temel JS, El-Jawahri A, LeBlanc TW. Palliative care and coping in patients with acute myeloid leukemia: Mediation analysis of data from a randomized clinical trial. Cancer. 2021 Dec 15;127(24):4702-4710. doi: 10.1002/cncr.33886. Epub 2021 Aug 30. PMID: 34460937; PMCID: PMC8664993.
Copy Download .nbib Format: NLM
Phase separation in fluids with many interacting components.

Proceedings of the National Academy of Sciences of the United States of America

Shrinivas K, Brenner MP.
PMID: 34725154
Proc Natl Acad Sci U S A. 2021 Nov 09;118(45). doi: 10.1073/pnas.2108551118.

Fluids in natural systems, like the cytoplasm of a cell, often contain thousands of molecular species that are organized into multiple coexisting phases that enable diverse and specific functions. How interactions between numerous molecular species encode for various emergent...

Cite
Shrinivas K, Brenner MP. Phase separation in fluids with many interacting components. Proc Natl Acad Sci U S A. 2021;118(45)doi: 10.1073/pnas.2108551118.
Shrinivas, K., & Brenner, M. P. (2021). Phase separation in fluids with many interacting components. Proceedings of the National Academy of Sciences of the United States of America, 118(45), . https://doi.org/10.1073/pnas.2108551118
Shrinivas, Krishna, and Brenner, Michael P. "Phase separation in fluids with many interacting components." Proceedings of the National Academy of Sciences of the United States of America vol. 118,45 (2021). doi: https://doi.org/10.1073/pnas.2108551118
Shrinivas K, Brenner MP. Phase separation in fluids with many interacting components. Proc Natl Acad Sci U S A. 2021 Nov 09;118(45). doi: 10.1073/pnas.2108551118. PMID: 34725154; PMCID: PMC8609339.
Copy Download .nbib Format: NLM
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.

European journal of human genetics : EJHG

Zurek B, Ellwanger K, Vissers LELM, Schüle R, Synofzik M, Töpf A, de Voer RM, Laurie S, Matalonga L, Gilissen C, Ossowski S, 't Hoen PAC, Vitobello A, Schulze-Hentrich JM, Riess O, Brunner HG, Brookes AJ, Rath A, Bonne G, Gumus G, Verloes A, Hoogerbrugge N, Evangelista T, Harmuth T, Swertz M, Spalding D, Hoischen A, Beltran S, Graessner H.
PMID: 34385672
Eur J Hum Genet. 2021 Sep;29(9):1459-1461. doi: 10.1038/s41431-021-00936-4.

No abstract available.

Cite
Zurek B, Ellwanger K, Vissers LELM, et al. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. Eur J Hum Genet. 2021;29(9):1459-1461doi: 10.1038/s41431-021-00936-4.
Zurek, B., Ellwanger, K., Vissers, L. E. L. M., Schüle, R., Synofzik, M., Töpf, A., de Voer, R. M., Laurie, S., Matalonga, L., Gilissen, C., Ossowski, S., 't Hoen, P. A. C., Vitobello, A., Schulze-Hentrich, J. M., Riess, O., Brunner, H. G., Brookes, A. J., Rath, A., Bonne, G., Gumus, G., Verloes, A., Hoogerbrugge, N., Evangelista, T., Harmuth, T., Swertz, M., Spalding, D., Hoischen, A., Beltran, S., Graessner, H. (2021). Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. European journal of human genetics : EJHG, 29(9), 1459-1461. https://doi.org/10.1038/s41431-021-00936-4
Zurek, Birte, et al. "Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases." European journal of human genetics : EJHG vol. 29,9 (2021): 1459-1461. doi: https://doi.org/10.1038/s41431-021-00936-4
Zurek B, Ellwanger K, Vissers LELM, Schüle R, Synofzik M, Töpf A, de Voer RM, Laurie S, Matalonga L, Gilissen C, Ossowski S, 't Hoen PAC, Vitobello A, Schulze-Hentrich JM, Riess O, Brunner HG, Brookes AJ, Rath A, Bonne G, Gumus G, Verloes A, Hoogerbrugge N, Evangelista T, Harmuth T, Swertz M, Spalding D, Hoischen A, Beltran S, Graessner H. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. Eur J Hum Genet. 2021 Sep;29(9):1459-1461. doi: 10.1038/s41431-021-00936-4. PMID: 34385672; PMCID: PMC8440583.
Copy Download .nbib Format: NLM
Decoding onset and direction of movements using Electrocorticographic (ECoG) signals in humans.

Frontiers in neuroengineering

Wang Z, Gunduz A, Brunner P, Ritaccio AL, Ji Q, Schalk G.
PMID: 22891058
Front Neuroeng. 2012 Aug 08;5:15. doi: 10.3389/fneng.2012.00015. eCollection 2012.

Communication of intent usually requires motor function. This requirement can be limiting when a person is engaged in a task, or prohibitive for some people suffering from neuromuscular disorders. Determining a person's intent, e.g., where and when to move,...

Cite
Wang Z, Gunduz A, Brunner P, et al. Decoding onset and direction of movements using Electrocorticographic (ECoG) signals in humans. Front Neuroeng. 2012;5:15doi: 10.3389/fneng.2012.00015.
Wang, Z., Gunduz, A., Brunner, P., Ritaccio, A. L., Ji, Q., & Schalk, G. (2012). Decoding onset and direction of movements using Electrocorticographic (ECoG) signals in humans. Frontiers in neuroengineering, 515. https://doi.org/10.3389/fneng.2012.00015
Wang, Zuoguan, et al. "Decoding onset and direction of movements using Electrocorticographic (ECoG) signals in humans." Frontiers in neuroengineering vol. 5 (2012): 15. doi: https://doi.org/10.3389/fneng.2012.00015
Wang Z, Gunduz A, Brunner P, Ritaccio AL, Ji Q, Schalk G. Decoding onset and direction of movements using Electrocorticographic (ECoG) signals in humans. Front Neuroeng. 2012 Aug 08;5:15. doi: 10.3389/fneng.2012.00015. eCollection 2012. PMID: 22891058; PMCID: PMC3413946.
Copy Download .nbib Format: NLM
[Incidental finding of tracheal system in a 23-year-old patient].

Deutsche medizinische Wochenschrift (1946)

Kloth C, Breining T, Brunner H.
PMID: 34344037
Dtsch Med Wochenschr. 2021 Aug;146(15):1003-1004. doi: 10.1055/a-1523-8668. Epub 2021 Aug 03.

No abstract available.

Cite
Kloth C, Breining T, Brunner H. Zufallsbefund am Trachealsystem bei einem 23-jährigen Patienten. [Incidental finding of tracheal system in a 23-year-old patient]. Dtsch Med Wochenschr. 2021;146(15):1003-1004doi: 10.1055/a-1523-8668.
Kloth, C., Breining, T., & Brunner, H. (2021). Zufallsbefund am Trachealsystem bei einem 23-jährigen Patienten. [Incidental finding of tracheal system in a 23-year-old patient]. Deutsche medizinische Wochenschrift (1946), 146(15), 1003-1004. https://doi.org/10.1055/a-1523-8668
Kloth, Christopher, et al. "Zufallsbefund am Trachealsystem bei einem 23-jährigen Patienten." [Incidental finding of tracheal system in a 23-year-old patient]. Deutsche medizinische Wochenschrift (1946) vol. 146,15 (2021): 1003-1004. doi: https://doi.org/10.1055/a-1523-8668
Kloth C, Breining T, Brunner H. Zufallsbefund am Trachealsystem bei einem 23-jährigen Patienten. [Incidental finding of tracheal system in a 23-year-old patient]. Dtsch Med Wochenschr. 2021 Aug;146(15):1003-1004. doi: 10.1055/a-1523-8668. Epub 2021 Aug 03. German. PMID: 34344037.
Copy Download .nbib Format: NLM
Showing 25 to 36 of 318 entries