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Cardiac 123I-metaiodobenzylguanidine Scintigraphy in a Patient with Familial Parkinsonism with Parkin Gene Mutation
Young-Do Kim, In-Uk Song, Joong-Seok Kim, Sung-Woo Chung, Kwang-Soo Lee
JMD. 2010;3(2):42-44.     DOI: https://doi.org/10.14802/jmd.10011

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Cardiac <sup>123</sup>I-metaiodobenzylguanidine Scintigraphy in a Patient with Familial Parkinsonism with <italic>Parkin</italic> Gene Mutation
Journal of Movement Disorders. 2010;3(2):42-44   Crossref logo
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Usefulness of Somatostatin Receptor Scintigraphy (99mTc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography
Neuroendocrinology. 2015;101(4):321-330   Crossref logo
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2.125 CARDIAC 123I-METAIODOBENZYLGUANIDINE SCINTIGRAPHY IN PARKINSON'S DISEASE (PD) PATIENTS WITH SCANS WITHOUT EVIDENCE OF DOPAMINERGIC DEFICIT (SWEDDS)
Parkinsonism & Related Disorders. 2012;18:S107   Crossref logo
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The role of cardiac 123 I‐metaiodobenzylguanidine scintigraphy in multiple system atrophy
Psychogeriatrics. 2020;   Crossref logo
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Sympathetic Denervation of Myocardium Demonstrated by 123I-MIBG Scintigraphy in Pure Progressive Autonomic Failure
European Neurology. 1997;38(4):291-296   Crossref logo
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A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism
Neuroscience Letters. 2000;289(1):66-68   Crossref logo
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CAPABILITIES OF 123I-MIBG SCINTIGRAPHY AND GATED BLOOD-POOL SPECT IN PREDICTING THE RESULTS OF CARDIAC RESYNCHRONIZATION THERAPY
The Siberian Medical Journal. 2019;34(2):63-70   Crossref logo
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The Role of 123I-Metaiodobenzylguanidine Myocardial Scintigraphy in the Diagnosis of Lewy Body Disease in Patients with Dementia in a Memory Clinic
Dementia and Geriatric Cognitive Disorders. 2006;22(5-6):379-384   Crossref logo
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Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe110→Ile Mutation in Cardiac Troponin T
Cardiology. 2000;93(3):155-162   Crossref logo
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Successful treatment of Juvenile parkinsonism with bilateral subthalamic deep brain stimulation in a 14-year-old patient with parkin gene mutation
Parkinsonism & Related Disorders. 2016;24:137-138   Crossref logo
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