Ina Knerr

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 8

Top Topics

Top Venues

Journal of inherited metabolic disease

Journal of nutrition and metabolism

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

Publications

Fiona Boyle, Gary Lynch, Michelle L Kearns, Adam Green, Gemma Parr, Caoimhe Howard, Ina Knerr, Jane Rice
Determination of the Protein and Amino Acid Content of Fruit, Vegetables and Starchy Roots for Use in Inherited Metabolic Disorders. Nutrients 16 (17) (2024)
Ina Knerr, David Cassiman
Ornithine transcarbamylase deficiency: A diagnostic odyssey. Journal of inherited metabolic disease 45 (4) (2022)
Jason Foran, Michael Moore, Ellen Crushell, Ina Knerr, Niamh McSweeney
Low excretor glutaric aciduria type 1 of insidious onset with dystonia and atypical clinical features, a diagnostic dilemma. JIMD reports 58 (1) (2020)
Daniel O'Reilly, Ellen Crushell, Joanne Hughes, Stephanie Ryan, Yvonne Rogers, Ingrid Borovickova, Philip Mayne, Michael Riordan, Atif Awan, Kevin Carson, Kim Hunter, Bryan Lynch, Amre Shahwan, Véronique Rüfenacht, Johannes Häberle, Eileen P Treacy, Ahmad A Monavari, Ina Knerr
Maple syrup urine disease: Clinical outcomes, metabolic control, and genotypes in a screened population after four decades of newborn bloodspot screening in the Republic of Ireland. Journal of inherited metabolic disease 44 (3) (2020)
Ina Knerr, Roberto Colombo, Jill Urquhart, Ana Morais, Begona Merinero, Alfonso Oyarzabal, Belén Pérez, Simon A Jones, Rahat Perveen, Mary A Preece, Yvonne Rogers, Eileen P Treacy, Philip Mayne, Giuseppe Zampino, Sabrina MacKinnon, Evangeline Wassmer, Wyatt W Yue, Ian Robinson, Pilar Rodríguez-Pombo, Simon E Olpin, Siddharth Banka
Expanding the genetic and phenotypic spectrum of branched-chain amino acid transferase 2 deficiency. Journal of inherited metabolic disease 42 (5) (2019)
John Allen, Bronwyn Power, Aida Abedin, Orla Purcell, Ina Knerr, Ahmad Monavari
Plasma methionine concentrations and incidence of hypermethioninemic encephalopathy during infancy in a large cohort of 36 patients with classical homocystinuria in the Republic of Ireland. JIMD reports 47 (1) (2019)
Anne Clark, Deirdre Deverell, Emma Corcoran, Margaret Macauley, Nicola Newcombe, Peter Branagan, Aoife Coughlan, Eimear Daly, Aoibhin Moore Heslin, Ellen Crushell, Joanne Hughes, Ina Knerr, Ahmad Monavari
Finger Prick to Finger Tip: Use of Mobile Phone Technology to Send PKU Blood Results. Journal of nutrition and metabolism 2018 (2018)
Ina Knerr, Laurie Bernstein, Ellen Crushell, Siobhan O'Sullivan, Jörn Oliver Sass
Amino Acids and Inherited Amino Acid-Related Disorders. Journal of nutrition and metabolism 2018 (2018)