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Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls

Orphanet journal of rare diseases, 2016-06, Vol.11 (1), p.87-87, Article 87

2016

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Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

Orphanet journal of rare diseases, 2019-12, Vol.14 (1), p.285-285, Article 285

2019

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A simple parasitological technique to increase detection of Strongyloides stercoralis in Bolivian primary health care system

BMC primary care, 2022-11, Vol.23 (1), p.284-284, Article 284

2022

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Geographic differences in the distribution of parasitic infections in children of Bolivia

Parasite epidemiology and control, 2021-08, Vol.14, p.e00217, Article e00217

2021

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Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway

Journal of inherited metabolic disease, 2022-09, Vol.45 (5), p.952-962

2022

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Neuropsychological outcome of NTBC‐treated patients with tyrosinaemia type 1

Developmental medicine and child neurology, 2011-10, Vol.53 (10), p.962-964

2011

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Hereditary Tyrosinemia Type 1 Mice under Continuous Nitisinone Treatment Display Remnants of an Uncorrected Liver Disease Phenotype

Genes, 2023-03, Vol.14 (3), p.693

2023

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Oxidative Stress, Glutathione Metabolism, and Liver Regeneration Pathways Are Activated in Hereditary Tyrosinemia Type 1 Mice upon Short-Term Nitisinone Discontinuation

Genes, 2020-12, Vol.12 (1), p.3

2020

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Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

Genes & diseases, 2023-09, Vol.10 (5), p.1759-1762

2023

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Neonatal liver cirrhosis without iron overload caused by gestational alloimmune liver disease

Pediatrics (Evanston), 2012-04, Vol.129 (4), p.e1076-e1079

2012

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Effects of thirty elements on bone metabolism

Journal of trace elements in medicine and biology, 2015-10, Vol.32, p.86-106

2015

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Interest of Anorectal Manometry During Long-term Follow-up of Patients Operated on for Hirschsprung's Disease

Journal of neurogastroenterology and motility, 2018-01, Vol.24 (1), p.70-78

2018

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Left ventricular assist device as bridge to liver transplantation in a patient with propionic acidemia and cardiogenic shock

The Journal of pediatrics, 2011-05, Vol.158 (5), p.866-867

2011

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Age-Related Variations in Acylcarnitine and Free Carnitine Concentrations Measured by Tandem Mass Spectrometry

Clinical chemistry (Baltimore, Md.), 2005-04, Vol.51 (4), p.745-752

2005

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Interferon alfa therapy for chronic hepatitis B in children: A multinational randomized controlled trial

Gastroenterology (New York, N.Y. 1943), 1998-05, Vol.114 (5), p.988-995

1998

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Lower protein content in infant formula reduces BMI and obesity risk at school age: follow-up of a randomized trial

The American journal of clinical nutrition, 2014-05, Vol.99 (5), p.1041-1051

2014

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Lower protein in infant formula is associated with lower weight up to age 2 y: a randomized clinical trial

The American journal of clinical nutrition, 2009-06, Vol.89 (6), p.1836-1845

2009

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Rectal suction biopsy with calretinin immunohistochemistry in patients suspected with residual aganglionosis after operation for Hirschsprung disease

Journal of pediatric surgery, 2017-10, Vol.52 (10), p.1597-1601

2017

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Maternal Smoking during Pregnancy and DNA-Methylation in Children at Age 5.5 Years: Epigenome-Wide-Analysis in the European Childhood Obesity Project (CHOP)-Study

PloS one, 2016-05, Vol.11 (5), p.e0155554-e0155554

2016

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Long-Term Outcomes and Quality of Life in Patients after Soave Pull-Through Operation for Hirschsprung's Disease: An Observational Retrospective Study

European journal of pediatric surgery, 2018-10, Vol.28 (5), p.445-454

2018

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Effect of calcium and vitamin D on growth, rickets and Kashin–Beck disease in 0‐ to 5‐year‐old children in a rural area of central Tibet

Tropical medicine & international health, 2016-06, Vol.21 (6), p.768-775

2016

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Key features and clinical variability of COG6-CDG

Molecular genetics and metabolism, 2015-11, Vol.116 (3), p.163-170

2015

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Different protein intake in the first year and its effects on adiposity rebound and obesity throughout childhood: 11 years follow‐up of a randomized controlled trial

Pediatric obesity, 2022-12, Vol.17 (12), p.e12961-n/a

2022

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Is a semi-elemental diet better than a polymeric diet after congenital heart surgery?

European journal of pediatrics, 2020-03, Vol.179 (3), p.423-430

2020

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Infantile colic, prolonged crying and maternal postnatal depression

Acta Paediatrica, 2009-08, Vol.98 (8), p.1344-1348

2009

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Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls

Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

A simple parasitological technique to increase detection of Strongyloides stercoralis in Bolivian primary health care system

Geographic differences in the distribution of parasitic infections in children of Bolivia

Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway

Neuropsychological outcome of NTBC‐treated patients with tyrosinaemia type 1

Hereditary Tyrosinemia Type 1 Mice under Continuous Nitisinone Treatment Display Remnants of an Uncorrected Liver Disease Phenotype

Oxidative Stress, Glutathione Metabolism, and Liver Regeneration Pathways Are Activated in Hereditary Tyrosinemia Type 1 Mice upon Short-Term Nitisinone Discontinuation

Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

Neonatal liver cirrhosis without iron overload caused by gestational alloimmune liver disease

Effects of thirty elements on bone metabolism

Interest of Anorectal Manometry During Long-term Follow-up of Patients Operated on for Hirschsprung's Disease

Left ventricular assist device as bridge to liver transplantation in a patient with propionic acidemia and cardiogenic shock

Age-Related Variations in Acylcarnitine and Free Carnitine Concentrations Measured by Tandem Mass Spectrometry

Interferon alfa therapy for chronic hepatitis B in children: A multinational randomized controlled trial

Lower protein content in infant formula reduces BMI and obesity risk at school age: follow-up of a randomized trial

Lower protein in infant formula is associated with lower weight up to age 2 y: a randomized clinical trial

Rectal suction biopsy with calretinin immunohistochemistry in patients suspected with residual aganglionosis after operation for Hirschsprung disease

Maternal Smoking during Pregnancy and DNA-Methylation in Children at Age 5.5 Years: Epigenome-Wide-Analysis in the European Childhood Obesity Project (CHOP)-Study

Long-Term Outcomes and Quality of Life in Patients after Soave Pull-Through Operation for Hirschsprung's Disease: An Observational Retrospective Study

Effect of calcium and vitamin D on growth, rickets and Kashin–Beck disease in 0‐ to 5‐year‐old children in a rural area of central Tibet

Key features and clinical variability of COG6-CDG

Different protein intake in the first year and its effects on adiposity rebound and obesity throughout childhood: 11 years follow‐up of a randomized controlled trial

Is a semi-elemental diet better than a polymeric diet after congenital heart surgery?

Infantile colic, prolonged crying and maternal postnatal depression

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