Adrienne Hammill

Associate Professor

Cincinnati Children's Hospital Medical Center

United States

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About

Adrienne Hammill is an Associate Professor at Cincinnati Children's Hospital Medical Center in the United States. Her research focuses on vascular anomalies, particularly in relation to the RAS pathway, and the management of lymphatic malformations. She has contributed to the standardization of terminology for hereditary hemorrhagic telangiectasia and has investigated brain vascular malformations associated with this condition.

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2023

Collaborators (8)

Dilini Vethanayagam

Professor

University of Alberta

CANADA

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Roshni Dasgupta

UNITED STATES

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Charles McCulloch

University of California, San Francisco

UNITED STATES

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Stryder Meadows

Tulane University

UNITED STATES

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Ilona Frieden

Professor

University of California, San Francisco

UNITED STATES

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Timothy Le Cras

Associate Professor

Cincinnati Children's Hospital Medical Center

UNITED STATES

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Michael Jeng

Professor

Stanford University School of Medicine

UNITED STATES

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Clifford Weiss

Professor

Johns Hopkins University School of Medicine

UNITED STATES

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Adrienne Hammill

Research Interests

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About

Articles (25)

Management, Trends, and Recommendations for Intra-abdominal Lymphatic Malformations: A Single-Center Retrospective Review

RAS Pathway Mutations and Therapeutics in Vascular Anomalies

Safety findings from the phase 1/2 MOSAIC study of miransertib for patients with PIK3CA-related overgrowth spectrum or Proteus syndrome

Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report

De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia

Current Practice: Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasia for Brain Vascular Malformations

Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia

Capillary malformations

Intra-Abdominal Lymphatic Malformations

Longitudinal prospective study of Sturge–Weber syndrome urine angiogenic factors and neurological outcome

Longitudinal prospective study of Sturge–Weber syndrome urine angiogenic factors and neurological outcome

Prevalence and Predictors of Hereditary Hemorrhagic Telangiectasia and Capillary-Malformation Arteriovenous Malformation Syndrome Among Children with Neurovascular Malformations

Prevalence and Predictors of Hereditary Hemorrhagic Telangiectasia and Capillary-Malformation Arteriovenous Malformation Syndrome Among Children with Neurovascular Malformations

Epik-P2: A Phase 2 Study of Alpelisib (ALP) in Pediatric and Adult Patients (pts) with<i> PIK3CA</i>-Related Overgrowth Spectrum (PROS)

Hereditary hemorrhagic telangiectasia - pediatric review

Genetic testing in the evaluation of individuals with clinical diagnosis of atypical Sturge–Weber syndrome

Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT

Kaposiform lymphangiomatosis: Diagnosis, pathogenesis, and treatment.

Response to sirolimus in capillary lymphatic venous malformations and associated syndromes: Impact on symptomatology, quality of life, and radiographic response

Executive summary of the 14th HHT international scientific conference

The Role of Hereditary Hemorrhagic Telangiectasia in Neurologic Practice

Vascular Anomalies Care in the United States: A Cross-sectional National Survey

Vascular Anomalies Care in the United States: A Cross-Sectional National Survey

An analysis of sex differences in pulmonary arteriovenous malformation presentation, complications and management in a large, multinational registry of patients with hereditary haemorrhagic telangiectasia

Barriers to Genetic Testing in Vascular Malformations

Collaborators (8)

Dilini Vethanayagam

Roshni Dasgupta

Charles McCulloch

Stryder Meadows

Ilona Frieden

Timothy Le Cras

Michael Jeng

Clifford Weiss

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