primary hyperoxaluria type i Latest Research Papers

Rapid Development of Renal Failure Following Simultaneous Liver and Kidney Transplantation in Two Siblings with Primary Hyperoxaluria Type I Due to c.473C>T(p.Ser158Leu) Genotype

Journal of Liver Transplantation ◽

10.1016/j.liver.2021.100020 ◽

2021 ◽

pp. 100020

Author(s):

Ahmed M. Alkhunaizi ◽

Nouriya Al-Sannaa

Keyword(s):

Renal Failure ◽

Kidney Transplantation ◽

Rapid Development ◽

Primary Hyperoxaluria ◽

Type I ◽

Primary Hyperoxaluria Type ◽

Liver And Kidney ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Outcomes of comprehensive management for 11 Chinese pediatric primary hyperoxaluria type I patients

European Urology Open Science ◽

10.1016/s2666-1683(20)34007-6 ◽

2020 ◽

Vol 19 ◽

pp. e2087

Author(s):

Z. Fangzhou ◽

Li Jun

Keyword(s):

Primary Hyperoxaluria ◽

Type I ◽

Comprehensive Management ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Plasma oxalate levels in primary hyperoxaluria type I show significant intra-individual variation and do not correlate with kidney function

Pediatric Nephrology ◽

10.1007/s00467-020-04531-5 ◽

2020 ◽

Vol 35 (7) ◽

pp. 1227-1233

Author(s):

Philip Hillebrand ◽

Bernd Hoppe

Keyword(s):

Kidney Function ◽

Individual Variation ◽

Primary Hyperoxaluria ◽

Type I ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Primary Hyperoxaluria Type I

10.32388/sh6ons ◽

2020 ◽

Author(s):

Keyword(s):

Primary Hyperoxaluria ◽

Type I ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.

Stem Cell Research ◽

10.1016/j.scr.2019.101626 ◽

2019 ◽

Vol 41 ◽

pp. 101626

Author(s):

Rebeca Martinez-Turrillas ◽

Saray Rodriguez-Diaz ◽

Paula Rodriguez-Marquez ◽

Angel Martin-Mallo ◽

Eduardo Salido ◽

...

Keyword(s):

Primary Hyperoxaluria ◽

Induced Pluripotent Stem Cell ◽

Compound Heterozygous ◽

Type I ◽

Stem Cell Line ◽

Hyperoxaluria Type I ◽

Induced Pluripotent ◽

Primary Hyperoxaluria Type I ◽

Agxt Gene ◽

Hyperoxaluria Type

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Same Donor Laparoscopic Liver and Kidney Procurement for Sequential Living Donor Liver–Kidney Transplantation in Primary Hyperoxaluria Type I

Journal of Laparoendoscopic & Advanced Surgical Techniques ◽

10.1089/lap.2019.0483 ◽

2019 ◽

Vol 29 (12) ◽

pp. 1616-1622

Author(s):

Roberta Angelico ◽

Isabella Guzzo ◽

Marco Pellicciaro ◽

Maria Cristina Saffioti ◽

Chiara Grimaldi ◽

...

Keyword(s):

Kidney Transplantation ◽

Living Donor ◽

Primary Hyperoxaluria ◽

Type I ◽

Donor Liver ◽

Primary Hyperoxaluria Type ◽

Liver And Kidney ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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769 – Identifying Small Molecules to Correct Abnormal Protein Trafficking of Alanine-Glyoxylate Aminotransferase (AGT) in a Human Cell Model of Primary Hyperoxaluria Type I to Avoid Need for Liver Transplantation

Gastroenterology ◽

10.1016/s0016-5085(19)40020-6 ◽

2019 ◽

Vol 156 (6) ◽

pp. S-1214-S-1215

Author(s):

Jordan S. Whatley ◽

Carla M. Koehler

Keyword(s):

Small Molecules ◽

Protein Trafficking ◽

Cell Model ◽

Primary Hyperoxaluria ◽

Type I ◽

Abnormal Protein ◽

Hyperoxaluria Type I ◽

Glyoxylate Aminotransferase ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Re: CRISPR/Cas9-Mediated Glycolate Oxidase Disruption is an Efficacious and Safe Treatment for Primary Hyperoxaluria Type I

The Journal of Urology ◽

10.1097/01.ju.0000554109.94248.01 ◽

2019 ◽

Vol 201 (5) ◽

pp. 853-854

Author(s):

Dean G. Assimos

Keyword(s):

Primary Hyperoxaluria ◽

Glycolate Oxidase ◽

Type I ◽

Safe Treatment ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation

Frontiers in Pharmacology ◽

10.3389/fphar.2019.00085 ◽

2019 ◽

Vol 10 ◽

Cited By ~ 2

Author(s):

Xiulan Lu ◽

Weijian Chen ◽

Liping Li ◽

Xinyuan Zhu ◽

Caizhi Huang ◽

...

Keyword(s):

Primary Hyperoxaluria ◽

Chinese Family ◽

Type I ◽

Infantile Form ◽

Family Research ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I

Molecular Chaperones in Human Disorders - Advances in Protein Chemistry and Structural Biology ◽

10.1016/bs.apcsb.2018.09.003 ◽

2019 ◽

pp. 119-152 ◽

Cited By ~ 4

Author(s):

José Ángel Fernández-Higuero ◽

Isabel Betancor-Fernández ◽

Noel Mesa-Torres ◽

Arturo Muga ◽

Eduardo Salido ◽

...

Keyword(s):

Molecular Chaperones ◽

Primary Hyperoxaluria ◽

Type I ◽

Primary Hyperoxaluria Type ◽

Hyperoxaluria Type I ◽

Primary Hyperoxaluria Type I ◽

Hyperoxaluria Type

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primary hyperoxaluria type i
Recently Published Documents

TOTAL DOCUMENTS

H-INDEX

Rapid Development of Renal Failure Following Simultaneous Liver and Kidney Transplantation in Two Siblings with Primary Hyperoxaluria Type I Due to c.473C>T(p.Ser158Leu) Genotype

Outcomes of comprehensive management for 11 Chinese pediatric primary hyperoxaluria type I patients

Plasma oxalate levels in primary hyperoxaluria type I show significant intra-individual variation and do not correlate with kidney function

Primary Hyperoxaluria Type I

Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.

Same Donor Laparoscopic Liver and Kidney Procurement for Sequential Living Donor Liver–Kidney Transplantation in Primary Hyperoxaluria Type I

769 – Identifying Small Molecules to Correct Abnormal Protein Trafficking of Alanine-Glyoxylate Aminotransferase (AGT) in a Human Cell Model of Primary Hyperoxaluria Type I to Avoid Need for Liver Transplantation

Re: CRISPR/Cas9-Mediated Glycolate Oxidase Disruption is an Efficacious and Safe Treatment for Primary Hyperoxaluria Type I

Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation

Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I

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primary hyperoxaluria type iRecently Published Documents

TOTAL DOCUMENTS

H-INDEX

Rapid Development of Renal Failure Following Simultaneous Liver and Kidney Transplantation in Two Siblings with Primary Hyperoxaluria Type I Due to c.473C>T(p.Ser158Leu) Genotype

Outcomes of comprehensive management for 11 Chinese pediatric primary hyperoxaluria type I patients

Plasma oxalate levels in primary hyperoxaluria type I show significant intra-individual variation and do not correlate with kidney function

Primary Hyperoxaluria Type I

Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.

Same Donor Laparoscopic Liver and Kidney Procurement for Sequential Living Donor Liver–Kidney Transplantation in Primary Hyperoxaluria Type I

769 – Identifying Small Molecules to Correct Abnormal Protein Trafficking of Alanine-Glyoxylate Aminotransferase (AGT) in a Human Cell Model of Primary Hyperoxaluria Type I to Avoid Need for Liver Transplantation

Re: CRISPR/Cas9-Mediated Glycolate Oxidase Disruption is an Efficacious and Safe Treatment for Primary Hyperoxaluria Type I

Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation

Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I

primary hyperoxaluria type i
Recently Published Documents