[Monofactorial heredity]

Same author

Long-Term Follow-Up of Patients With Transaldolase Deficiency.

Journal of inherited metabolic disease·2026

Same author

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature.

Epileptic disorders : international epilepsy journal with videotape·2025

Same author

Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.

Molecular genetics and metabolism·2023

Same author

Clinical phenotype associated with TANGO2 gene mutation.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2020

Same author

Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2020

Same author

Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults.

Revue neurologique·2020

Same journal

[Prolonged fever].

La Revue du praticien·2026

Same journal

[Lower gastrointestinal bleeding].

La Revue du praticien·2026

Same journal

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

La Revue du praticien·2026

Same journal

[A history of child abuse intervention in the West].

La Revue du praticien·2026

Same journal

[Agranulocytose médicamenteuse].

La Revue du praticien·2026

Same journal

[Patient education in heart failure].

La Revue du praticien·2026

Related Experiment Videos

[Monofactorial heredity]

Related Concept Videos

Long-Term Follow-Up of Patients With Transaldolase Deficiency.

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature.

Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.

Clinical phenotype associated with TANGO2 gene mutation.

Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis.

Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults.

[Prolonged fever].

[Lower gastrointestinal bleeding].

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

[A history of child abuse intervention in the West].

[Agranulocytose médicamenteuse].

[Patient education in heart failure].

Related Experiment Videos

[Monofactorial heredity]

Related Concept Videos

Related Articles

Long-Term Follow-Up of Patients With Transaldolase Deficiency.

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature.

Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.

Clinical phenotype associated with TANGO2 gene mutation.

Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis.

Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults.

[Prolonged fever].

[Lower gastrointestinal bleeding].

[Management of antiplatelet agents and oral anticoagulants in cases of gastrointestinal bleeding].

[A history of child abuse intervention in the West].

[Agranulocytose médicamenteuse].

[Patient education in heart failure].