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Neurosurgical Focus
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January 1, 2025
Craniosynostosis as a cause of intracranial hypertension in Alagille syndrome: a case series of 6 consecutive pediatric patients
Lelio Guida, Antoine Gardin, Syril James, et al.
Communications Biology
|
July 24, 2024
Identification of new correctors for traffic-defective ABCB4 variants by a high-content screening approach
Mounia Lakli, Julie Dumont, Virginie Vauthier, et al.
Molecular Genetics and Metabolism
|
December 14, 2020
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia
Pierre-Hadrien Becker, Zeynep Demir, Yael Mozer Glassberg, et al.
Journal of Hepatology
|
November 17, 2009
ATP release after partial hepatectomy regulates liver regeneration in the rat
Emmanuel Gonzales, Boris Julien, Valérie Serrière-Lanneau, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
March 2, 2021
Effect of CFTR correctors on the traffic and the function of intracellularly retained ABCB4 variants
Amel Ben Saad, Virginie Vauthier, Ágota Tóth, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
March 8, 2017
Attempt to Determine the Prevalence of Two Inborn Errors of Primary Bile Acid Synthesis: Results of a European Survey
Jörg Jahnel, Evelyn Zöhrer, Björn Fischler, et al.
JHEP Reports : Innovation in Hepatology
|
February 21, 2025
Placental growth factor modulates endothelial NO production and exacerbates experimental hepatopulmonary syndrome
Fabien Robert, Feriel Benchenouf, My Ngoc Ha, et al.
Diagnostics (Basel, Switzerland)
|
May 28, 2022
Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis
Marion Almes, Anne Spraul, Mathias Ruiz, et al.
JHEP Reports : Innovation in Hepatology
|
September 13, 2023
Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy
Emmanuel Gonzales, Antoine Gardin, Marion Almes, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2022
International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts
Simona Korff, Khaled Mostaguir, Maurice Beghetti, et al.
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of 10
Search research articles
Search
Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
Neurosurgical Focus
|
January 1, 2025
Craniosynostosis as a cause of intracranial hypertension in Alagille syndrome: a case series of 6 consecutive pediatric patients
Lelio Guida, Antoine Gardin, Syril James, et al.
Communications Biology
|
July 24, 2024
Identification of new correctors for traffic-defective ABCB4 variants by a high-content screening approach
Mounia Lakli, Julie Dumont, Virginie Vauthier, et al.
Molecular Genetics and Metabolism
|
December 14, 2020
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia
Pierre-Hadrien Becker, Zeynep Demir, Yael Mozer Glassberg, et al.
Journal of Hepatology
|
November 17, 2009
ATP release after partial hepatectomy regulates liver regeneration in the rat
Emmanuel Gonzales, Boris Julien, Valérie Serrière-Lanneau, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
March 2, 2021
Effect of CFTR correctors on the traffic and the function of intracellularly retained ABCB4 variants
Amel Ben Saad, Virginie Vauthier, Ágota Tóth, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
March 8, 2017
Attempt to Determine the Prevalence of Two Inborn Errors of Primary Bile Acid Synthesis: Results of a European Survey
Jörg Jahnel, Evelyn Zöhrer, Björn Fischler, et al.
JHEP Reports : Innovation in Hepatology
|
February 21, 2025
Placental growth factor modulates endothelial NO production and exacerbates experimental hepatopulmonary syndrome
Fabien Robert, Feriel Benchenouf, My Ngoc Ha, et al.
Diagnostics (Basel, Switzerland)
|
May 28, 2022
Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis
Marion Almes, Anne Spraul, Mathias Ruiz, et al.
JHEP Reports : Innovation in Hepatology
|
September 13, 2023
Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy
Emmanuel Gonzales, Antoine Gardin, Marion Almes, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2022
International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts
Simona Korff, Khaled Mostaguir, Maurice Beghetti, et al.
Page
of 10