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Repair: The Interface Between Interaction and Cognition

Topics in cognitive science, 2018-04, Vol.10 (2), p.279-313

2018

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Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: A review

Journal of inherited metabolic disease, 2008-04, Vol.31 (2), p.205-216

2008

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Projecting the end of a Speaker's Turn: A Cognitive Cornerstone of Conversation

Language (Baltimore), 2006-09, Vol.82 (3), p.515-535

2006

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An Appeal for a Methodological Fusion of Conversation Analysis and Experimental Psychology

Research on language and social interaction, 2017-01, Vol.50 (1), p.90-107

2017

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Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy

American journal of human genetics, 2007-12, Vol.81 (6), p.1133-1143

2007

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Clinical variability of isovaleric acidemia in a genetically homogeneous population

Journal of inherited metabolic disease, 2012-11, Vol.35 (6), p.1021-1029

2012

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Primary and secondary pragmatic functions of pointing gestures

Journal of pragmatics, 2007-10, Vol.39 (10), p.1722-1741

2007

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Improving Human Interaction Research through Ecological Grounding

Collabra. Psychology, 2018-07, Vol.4 (1)

2018

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Prediction of turn-ends based on anticipation of upcoming words

Frontiers in psychology, 2012-01, Vol.3, p.376-376

2012

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Estimating Systemic Cognitive States from a Mixture of Physiological and Brain Signals

Topics in cognitive science, 2023-06

2023

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Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy

Pediatric research, 2000, Vol.47 (1), p.43-45

2000

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A biological infrastructure for communication underlies the cultural evolution of languages

The Behavioral and brain sciences, 2008-10, Vol.31 (5), p.518-518

2008

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Cognitive and social delays in the initiation of conversational repair

Dialogue and discourse, 2021, Vol.12 (1), p.21-44

2021

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High activity of fatty acid oxidation enzymes in human placenta: Implications for fetal‐maternal disease

Journal of inherited metabolic disease, 2003-01, Vol.26 (4), p.385-392

2003

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Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders

Human molecular genetics, 2005-09, Vol.14 (18), p.2695-2703

2005

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2‐Methyl‐3‐hydroxybutyryl‐CoA dehydrogenase deficiency in a 23‐year‐old man

Journal of inherited metabolic disease, 2002-11, Vol.25 (6), p.477-482

2002

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An evaluation of two alongshore transport equations with field measurements

Coastal engineering (Amsterdam), 2009-03, Vol.56 (3), p.313-319

2009

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Carnitine supplementation induces long‐chain acylcarnitine production—Studies in the VLCAD‐deficient mouse

Journal of inherited metabolic disease, 2006-04, Vol.29 (2-3), p.343-344

2006

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Parallelism in the Production of Noun Phrases: Experiments and Reaction Time Models

Journal of experimental psychology. Learning, memory, and cognition, 1999-05, Vol.25 (3), p.702-720

1999

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Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain

Biochemical and biophysical research communications, 2006-07, Vol.346 (1), p.33-37

2006

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Onshore sandbar migration at Tairua Beach (New Zealand): Numerical simulations and field measurements

Marine geology, 2008-08, Vol.253 (3), p.99-106

2008

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Succinyl-CoA :acetoacetate transferase deficiency : identification of a new patient with a neonatal onset and review of the literature

European journal of pediatrics, 1997-11, Vol.156 (11), p.870-873

1997

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Thermo‐sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy

Journal of inherited metabolic disease, 2022-07, Vol.45 (4), p.819-831

2022

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Lactic acidosis in long‐chain fatty acid β‐oxidation disorders

Journal of inherited metabolic disease, 1998-08, Vol.21 (6), p.645-654

1998

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A new case of succinyl‐CoA:acetoacetate transferase deficiency: Favourable course despite very low residual activity

Journal of inherited metabolic disease, 2001-02, Vol.24 (1), p.81-82

2001

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Repair: The Interface Between Interaction and Cognition

Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: A review

Projecting the end of a Speaker's Turn: A Cognitive Cornerstone of Conversation

An Appeal for a Methodological Fusion of Conversation Analysis and Experimental Psychology

Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy

Clinical variability of isovaleric acidemia in a genetically homogeneous population

Primary and secondary pragmatic functions of pointing gestures

Improving Human Interaction Research through Ecological Grounding

Prediction of turn-ends based on anticipation of upcoming words

Estimating Systemic Cognitive States from a Mixture of Physiological and Brain Signals

Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy

A biological infrastructure for communication underlies the cultural evolution of languages

Cognitive and social delays in the initiation of conversational repair

High activity of fatty acid oxidation enzymes in human placenta: Implications for fetal‐maternal disease

Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders

2‐Methyl‐3‐hydroxybutyryl‐CoA dehydrogenase deficiency in a 23‐year‐old man

An evaluation of two alongshore transport equations with field measurements

Carnitine supplementation induces long‐chain acylcarnitine production—Studies in the VLCAD‐deficient mouse

Parallelism in the Production of Noun Phrases: Experiments and Reaction Time Models

Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain

Onshore sandbar migration at Tairua Beach (New Zealand): Numerical simulations and field measurements

Succinyl-CoA :acetoacetate transferase deficiency : identification of a new patient with a neonatal onset and review of the literature

Thermo‐sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy

Lactic acidosis in long‐chain fatty acid β‐oxidation disorders

A new case of succinyl‐CoA:acetoacetate transferase deficiency: Favourable course despite very low residual activity

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