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Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndrome

Genetics in medicine, 2020-12, Vol.22 (12), p.2101-2107

2020

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P051: Distribution of variants and tumor presentation in pediatric patients diagnosed with hereditary pheochromocytoma paraganglioma syndrome

Genetics in Medicine Open, 2023, Vol.1 (1), p.100070, Article 100070

2023

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P083: Incidental findings in FH and SDHA genes: Navigating cancer risk assessment and follow-up recommendations

Genetics in Medicine Open, 2023, Vol.1 (1), p.100102, Article 100102

2023

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Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50

Clinical endocrinology (Oxford), 2021-09, Vol.95 (3), p.447-452

2021

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PD58-02 GENOTYPE-PHENOTYPE ASSOCIATIONS IN VON HIPPEL-LINDAU SYNDROME: IMPLICATIONS FOR SCREENING

The Journal of urology, 2024-05, Vol.211 (5S)

2024

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Management of bilateral head and neck paragangliomas at a single-institution across four decades

Head & neck, 2024-08

2024

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Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple Decades

JAMA otolaryngology-- head & neck surgery, 2019-07, Vol.145 (7), p.641

2019

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The Natural History of Observed SDHx-Related Head and Neck Paragangliomas Using Three-Dimensional Volumetric Tumor Analysis

Otology & neurotology, 2023-10

2023

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Tumor detection rates in screening carriers with SDHx -related hereditary paraganglioma-pheochromocytoma syndrome based on prior tumor history

Journal of clinical oncology, 2020-05, Vol.38 (15_suppl), p.1545-1545

2020

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Evaluating Patterns of SDHx Tumor Presentation by Gene and Variant Type: A Retrospective Analysis of a Large Clinical Cohort

JCO precision oncology, 2023-09 (7)

2023

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Abstract 2559: Genotype-phenotype associations in von hippel-lindau syndrome: Implications for screening

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.2559-2559

2024

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Description of a SDHD c.129G>A (p.W43X) Mutation With Variable Presentation in Multiple Family Members

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A995-A995

2021

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Gliomas in the context of Li-Fraumeni syndrome: An international cohort

Journal of clinical oncology, 2019-05, Vol.37 (15_suppl), p.1517-1517

2019

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Abstract IA004: Risk of therapy-related subsequent cancers in individuals with germline TP53 variants

Cancer research (Chicago, Ill.), 2024-09, Vol.84 (17_Supplement), p.IA004-IA004

2024

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The dif Resolvase Locus of the Escherichia coli Chromosome can be Replaced by a 33-bp Sequence, but Function Depends on Location

Proceedings of the National Academy of Sciences - PNAS, 1995-02, Vol.92 (5), p.1352-1356

1995

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Predictable information in neural signals during resting state is reduced in autism spectrum disorder

Human brain mapping, 2018-08, Vol.39 (8), p.3227-3240

2018

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Being user-oriented: Convergences, divergences, and the potentials for systematic dialogue between disciplines and between researchers, designers, and providers

Proceedings of the American Society for Information Science and Technology, 2006, Vol.43 (1), p.1-9

2006

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Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma–pheochromocytoma syndrome

P051: Distribution of variants and tumor presentation in pediatric patients diagnosed with hereditary pheochromocytoma paraganglioma syndrome

P083: Incidental findings in FH and SDHA genes: Navigating cancer risk assessment and follow-up recommendations

Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50

PD58-02 GENOTYPE-PHENOTYPE ASSOCIATIONS IN VON HIPPEL-LINDAU SYNDROME: IMPLICATIONS FOR SCREENING

Management of bilateral head and neck paragangliomas at a single-institution across four decades

Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple Decades

The Natural History of Observed SDHx-Related Head and Neck Paragangliomas Using Three-Dimensional Volumetric Tumor Analysis

Tumor detection rates in screening carriers with SDHx -related hereditary paraganglioma-pheochromocytoma syndrome based on prior tumor history

Evaluating Patterns of SDHx Tumor Presentation by Gene and Variant Type: A Retrospective Analysis of a Large Clinical Cohort

Abstract 2559: Genotype-phenotype associations in von hippel-lindau syndrome: Implications for screening

Description of a SDHD c.129G>A (p.W43X) Mutation With Variable Presentation in Multiple Family Members

Gliomas in the context of Li-Fraumeni syndrome: An international cohort

Abstract IA004: Risk of therapy-related subsequent cancers in individuals with germline TP53 variants

The dif Resolvase Locus of the Escherichia coli Chromosome can be Replaced by a 33-bp Sequence, but Function Depends on Location

Predictable information in neural signals during resting state is reduced in autism spectrum disorder

Being user-oriented: Convergences, divergences, and the potentials for systematic dialogue between disciplines and between researchers, designers, and providers

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