Suchergebnisse - "Kapplinger, Jamie D"

PubPharm (42)

1

Sublobar Resection, Stereotactic Body Radiation Therapy, and Percutaneous Ablation Provide Comparable Outcomes for Lung Metastasis-Directed Therapy

enthalten in: Chest | 2023

von Gits, H. | Khosravi Flanigan, M. | Kapplinger, J. | +24

2

Safety and Efficacy of CT-Guided Percutaneous Biopsy of Suspicious Subcentimeter Pelvic and Retroperitoneal Lymph Nodes Detected by 11C-Choline PET in Patients With Prostate Cancer

enthalten in: AJR. American journal of roentgenology | 2023

von Kapplinger, J. | Lima, L. | Packard, A. | +4

CommentIn: AJR Am J Roentgenol. 2023 Jan 4;:. - PMID 36598103

3

Response by Kapplinger et al to Letter Regarding Article, "Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation"

enthalten in: Circulation. Genomic and precision medicine | 2018

von Kapplinger, J. | Tester, D. | Ackerman, M.

CommentOn: Circ Genom Precis Med. 2018 Feb;11(2):e001424. - PMID 29453246

4

Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign

enthalten in: Heart rhythm | 2018

von Clemens, D. | Lentino, A. | Kapplinger, J. | +4

CommentIn: Heart Rhythm. 2018 Apr;15(4):562-563. - PMID 29317317

5

Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation

enthalten in: Circulation. Genomic and precision medicine | 2018

von Kapplinger, J. | Pundi, K. | Larson, N. | +5

CommentIn: Circ Genom Precis Med. 2018 Feb;11(2):e002072. - PMID 29453248

6

Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 channels may have wild-type function and not cause type 1 long QT syndrome : Do not rely solely on the genetic test company's interpretation

enthalten in: HeartRhythm case reports | 2018

von Paquin, A. | Ye, D. | Tester, D. | +3

7

Sudden infant death syndrome and inherited cardiac conditions

enthalten in: Nature reviews. Cardiology | 2017

von Baruteau, A. | Tester, D. | Kapplinger, J. | +2

8

Lidocaine attenuation testing : An in vivo investigation of putative LQT3-associated variants in the SCN5A-encoded sodium channel

enthalten in: Heart rhythm | 2017

von Anderson, H. | Bos, J. | Kapplinger, J. | +3

CommentIn: Heart Rhythm. 2017 Aug;14(8):1180-1181. - PMID 28495653

9

KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1

enthalten in: Journal of medical genetics | 2017

von Kapplinger, J. | Erickson, A. | Asuri, S. | +8

10

Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome : A Japanese Multicenter Registry

enthalten in: Circulation | 2017

von Yamagata, K. | Horie, M. | Aiba, T. | +26

CommentIn: Circulation. 2017 Dec 5;136(23):2287-2288. - PMID 29203569

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