Thomas Andrew Burrow - Cincinnati Children’s Hospital Medical Center

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论文共 76 篇作者统计合作学者相似作者

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Bradycardia and Acidosis in a Term Newborn

Carson Savrick,Megha Sharma,Andrew Burrow,Jared Beavers

NeoReviewsno. 3 (2024): e166-e168

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Characteristics and Management of US Pediatric Patients with Gaucher Disease from the Gaucher Outcome Survey

Ozlem Goker-Alpan,Andrew Burrow,Gregory M. Enns,Can Ficicioglu,Priya S. Kishnani,Damara Ortiz,Carlos E. Prada,Divya Vats,Neal J. Weinreb, Ian Robinson,Ravi R. Pathak,Ekaterina Wright,Jaco Botha,William R. Wilcox

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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DESIGN OF A PHASE 3 STUDY OF AAV-MEDIATED GENE TRANSFER OF ORNITHINE TRANSCARBAMYLASE (OTC) IN PATIENTS WITH LATE-ONSET OTC DEFICIENCY

Laura Konczal,Joshua Baker, Margreet Wagenmakers, Jean Baptiste Arnoux,T. Andrew Burrow,Marie Luz Couce,Mireia del Toro,Norberto Guelbert,Soledad Kleppe,Gerald S. Lipshutz,Nicola Longo, Shiro Matsumoto,Andreas Schulze,Janet Thomas,J. Lawrence Merritt

Molecular Genetics and Metabolism（2024）

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04145 Profound Hypotonia in a Newborn with Biallelic Δ-Aminolevulinic Acid Dehydratase (ALAD) Mutations

Alexis Roach, Hannah Barkley, Carissa Rodriquez,T Andrew Burrow,Karl E Anderson, Ankita Shukla

Poster 54 (2024)

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Development of a Metabolic Decompensation Event Severity Score for Patients with Propionic Acidemia or Methylmalonic Acidemia

Ethan J. Schwartz,Nicola Longo,Sue Perera,Carlo Dionisi-Vici,Mary Leuchars,Andrew Burrow,Temitayo Ajayi,Javier de las Heras,Geetanjoli Banerjee,Carlos Prada,M. Alex Bellenger,Olga Moshkovich,Vanja Sikirica

MOLECULAR GENETICS AND METABOLISMno. 4 (2024)

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O18: A Path Forward for Patients with Glycogen Branching Enzyme Deficiency: Consensus on Diagnosing and Managing Glycogen Storage Disease Type IV*

Rebecca Koch,Claudia Soler-Alfonso,Bridget Kiely,Akihiro Asai,Ariana Smith,Deeksha Bali, Peter Kang,Andrew Landstrom,H. Orhan Akman,T. Andrew Burrow,Jennifer Orthmann-Murphy, Deberah Goldman,Surekha Pendyal,Areeg El-Gharbawy,Stephanie Austin,Laura Case,Raphael Schiffmann,Michio Hirano,Priya Kishnani

Genetics in Medicine Openno. 1 (2023): 100114-100114

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Cns-symptomatic hyperammonemia following recombinant crisantaspase pseudomonas fluorescens (rylaze)

Paige Strebeck,Lauren Appell,Jason Farrar,Divyaswathi Citla-Sridhar,Erin Bennett,T. Andrew Burrow,Cristyn Branstetter,Joana Mack

PEDIATRIC BLOOD & CANCER (2023): S73-S73

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The Diagnosis and Management of Gaucher Disease in Pediatric Patients: Where Do We Go from Here

Neal J. Weinreb,Ozlem Goker-Alpan,Priya S. Kishnani,Nicola Longo,T. Andrew Burrow,John A. Bernat,Punita Gupta,Nadene Henderson,Helio Pedro,Carlos E. Prada,Divya Vats,Ravi R. Pathak,Ekaterina Wright,Can Ficicioglu

Molecular Genetics and Metabolism（2022）

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A pathogenic variant of the DNM1L mitochondrial gene associated with super-refractory status epilepticus (SE) in a 15-year-old female

N. Prabhu,K. Arya, P. Drake, N. Arulprakash, S. Cobb, C. Manbeck, E. Willis,T. Burrow, D. Fry,D. Samanta,F. Perkins

ANNALS OF NEUROLOGY（2022）

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