Andrea L Gropman (A L Gropman, Andrea Gropman)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 19

Top Venues

International journal of molecular sciences

Genes

Prenatal diagnosis

Nutrients

National Children's Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Children's Center Aug 01 2003

United States

Chief, Neurogenetics and Neurodevelopmental Disabilities :: Neurology

Publications

Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Martine Uittenbogaard, Andrea L Gropman, Matthew T Whitehead, Christine A Brantner, Eliana Gropman, Anne Chiaramello
Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency. International journal of molecular sciences 25 (3) (2024)
Mary P Hamzik, Andrea L Gropman, Michaela R Brooks, Sherida Powell, Teresa Sadeghin, Carole A Samango-Sprouse
The Effect of Hormonal Therapy on the Behavioral Outcomes in 47,XXY (Klinefelter Syndrome) between 7 and 12 Years of Age. Genes 14 (7) (2023)
Kosar Khaksari, Wei-Liang Chen, Andrea L Gropman
Review of Applications of Near-Infrared Spectroscopy in Two Rare Disorders with Executive and Neurological Dysfunction: UCD and PKU. Genes 13 (10) (2022)
Lillian M Lai, Andrea L Gropman, Matthew T Whitehead
MR Neuroimaging in Pediatric Inborn Errors of Metabolism. Diagnostics (Basel, Switzerland) 12 (4) (2022)
Kuntal Sen, Marc T DiSabella, Jennifer Harmon, Jeffrey A Strelzik, Andrea L Gropman
Gaps in Neurogenetics Education During Child Neurology Residency: Results of a National Survey. Journal of child neurology 37 (8-9) (2022)
Bigna Katrin Bölsterli, Eugen Boltshauser, Luigi Palmieri, Johannes Spenger, Michaela Brunner-Krainz, Felix Distelmaier, Peter Freisinger, Tobias Geis, Andrea L Gropman, Johannes Häberle, Julia Hentschel, Bruno Jeandidier, Daniela Karall, Boris Keren, Annick Klabunde-Cherwon, Vassiliki Konstantopoulou, Raimund Kottke, Francesco M Lasorsa, Christine Makowski, Cyril Mignot, Ruth Tuura O'Gorman, Vito Porcelli, René Santer, Kuntal Sen, Katja Steinbrücker, Steffen Syrbe, Matias Wagner, Andreas Ziegler, Thomas Zöggeler, Johannes Adalbert Mayr, Holger Prokisch, Saskia B Wortmann
Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier. Nutrients 14 (17) (2022)
Kuntal Sen, Jennifer Harmon, Andrea L Gropman
Select Ethical Aspects of Next-Generation Sequencing Tests for Newborn Screening and Diagnostic Evaluation of Critically Ill Newborns. International journal of neonatal screening 7 (4) (2021)
Meaghan McGowan, Carlos Ferreira, Matthew Whitehead, Sudeepta K Basu, Taeun Chang, Andrea L Gropman
The Application of Neurodiagnostic Studies to Inform the Acute Management of a Newborn Presenting With Sarbamoyl Shosphate Synthetase 1 Deficiency. Child neurology open 8 (2021)
E Barkovich, Andrea L Gropman
Late Onset Ornithine Transcarbamylase Deficiency Triggered by an Acute Increase in Protein Intake: A Review of 10 Cases Reported in the Literature. Case reports in genetics 2020 (2020)
Selena L Tran, Carole A Samango-Sprouse, Teresa Sadeghin, Sherida Powell, Andrea L Gropman
Hormonal replacement therapy and its potential influence on working memory and competency/adaptive functioning in 47,XXY (Klinefelter syndrome). American journal of medical genetics. Part A 179 (12) (2019)
Carole A Samango-Sprouse, Debra R Counts, Selena L Tran, Patricia C Lasutschinkow, Grace F Porter, Andrea L Gropman
Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome). The application of clinical genetics 12 (2019)
Carole A Samango-Sprouse, Grace F Porter, Patricia C Lasutschinkow, Selena L Tran, Teresa Sadeghin, Andrea L Gropman
Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs). Prenatal diagnosis 40 (4) (2019)
Carole A Samango-Sprouse, Colleen Keen, Teresa Sadeghin, Andrea L Gropman
The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome). Prenatal diagnosis 37 (5) (2017)
Christopher A Wassif, Lisa Kratz, Susan E Sparks, Courtney Wheeler, Simona Bianconi, Andrea L Gropman, Karim A Calis, Richard I Kelley, Elaine Tierney, Forbes D Porter
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 19 (3) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Andrea L Gropman (A L Gropman, Andrea Gropman)