Liver transplantation for glycogen storage disease types I, III, and IV - Wikidata - wikimedia - TriplyDB

Liver transplantation for glycogen storage disease types I, III, and IV

Liver transplantation for glycogen storage disease types I, III, and IV

http://www.wikidata.org/entity/Q33797826

about

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach Liver tumors in children with metabolic disorders Liver transplantation in glycogen storage disease type I Glycogen storage disease type III diagnosis and management guidelines Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy Bone marrow-derived cells require a functional glucose 6-phosphate transporter for normal myeloid functions Long-term efficacy following readministration of an adeno-associated virus vector in dogs with glycogen storage disease type Ia Glycogen storage disease type III in Inuit children Development of hepatocellular adenomas and carcinomas in mice with liver-specific G6Pase-α deficiency Glycogen storage diseases: new perspectives.Glycogen storage disease type I: pathophysiology of liver adenomas.Does type I truly dominate hepatic glycogen storage diseases in Korea?: a single center study Glycogen storage disease type I: indications for liver and/or kidney transplantation.Guidelines for management of glycogen storage disease type I - European Study on Glycogen Storage Disease Type I (ESGSD I).Neutropenia in type Ib glycogen storage disease Recombinant AAV-directed gene therapy for type I glycogen storage diseases.Regression of hepatocellular adenomas with strict dietary therapy in patients with glycogen storage disease type I.Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector.Preclinical Development of New Therapy for Glycogen Storage Diseases.Cardiac Involvement in Glycogen Storage Disease Type IV: Two Cases and the Two Ends of a Spectrum Glycogen storage disease type III-hepatocellular carcinoma a long-term complication?The SLC37 family of phosphate-linked sugar phosphate antiporters.Gene therapy for type I glycogen storage diseases Glucose-6-phosphate transporter gene therapy corrects metabolic and myeloid abnormalities in glycogen storage disease type Ib mice.Pathogenesis of growth failure and partial reversal with gene therapy in murine and canine Glycogen Storage Disease type Ia Generation of mice with a conditional allele for G6pc.Outcomes of liver transplantation for glycogen storage disease: a matched-control study and a review of literature.Focal nodular hyperplasia and hepatic adenoma: current diagnosis and management.Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.Gene therapy with helper-dependent adenoviral vectors: lessons from studies in large animal models.Liver transplantation for adenomatosis: European experience.Delivery of glucose-6-phosphatase in a canine model for glycogen storage disease, type Ia, with adeno-associated virus (AAV) vectors.Rescue administration of a helper-dependent adenovirus vector with long-term efficacy in dogs with glycogen storage disease type Ia.Early, sustained efficacy of adeno-associated virus vector-mediated gene therapy in glycogen storage disease type Ia.In search of proof-of-concept: gene therapy for glycogen storage disease type Ia.Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes.Liver Transplantation in a Myopathic Patient with Glycogen Storage Disease Type IIIa and Decompensated Cirrhosis.Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities.Glycogen Storage Disease Type IV and Early Implantation Defect: Early Trophoblastic Involvement Associated with a New GBE1 Mutation.Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I).

P2860

Q26751169-BCCABC6A-45B4-4189-8605-7FE7942A7FE9 Q26770292-A22FA8A6-84C5-46F8-8FA1-410E81915865 Q27013712-AB503CEE-13FD-47B6-AC24-EF53BC352B3E Q28287932-588FFB86-96EA-48A4-8D44-9EF7D24D410D Q28296663-28DF3249-1DCE-485C-AD1A-9292EE55C815 Q28513160-1797612B-1D90-4F1C-8831-B7121F077D43 Q33720634-BE322599-1950-44D2-936E-B07195BBD467 Q33759486-0F755346-1147-4A50-9B9A-05371C875055 Q34081768-B03072AF-D47B-46DF-8B3D-29463C7718CC Q34098766-B5151B98-DDD7-406A-A6FE-273ADE68DC60 Q34528044-1FEF0042-A980-4B1E-9315-CE16868A8B2D Q34923585-7D985FC6-7C60-44D1-85FA-0EB0C8CD476D Q34954595-D40E68A8-7A4B-460D-8D5C-139BFFE6457D Q34954705-33CEEF9A-E2CB-4BCE-B374-8A291DFC657C Q34996563-4FD5182C-FD46-4166-A5CE-BB402F6D9700 Q35078590-BA90FB69-081F-45ED-818D-067831AA6147 Q35183122-220E9095-C1EC-4EA6-80D7-7EE79878B32E Q35568513-45269F8C-0DE0-49EB-8325-E66733B30B19 Q35677604-8BF01A46-0DA9-4BD9-A1AD-8F723F0ABCC0 Q36296501-FF5636AA-B3BB-4904-8AC6-3ADC2D8F2060 Q36695473-60CBF067-EFA3-4796-9C8E-D962987A59F5 Q36700318-B58DEFDA-7424-40C7-9754-514DE7363846 Q36789527-DD2E5978-3D77-4FEE-AFED-6A62887EC283 Q36828787-F3E7FA4A-C9A7-40A8-B36C-5DAFAB8C9C5A Q37150574-9F38F67C-4921-4B07-9914-D02F4ADFF597 Q37371421-0E0ECD9A-87A7-4BDD-B240-D2C23733D9AF Q37953968-ACF8ED74-154B-48AA-8A28-7DD5966F93A8 Q38117581-F4C1CE75-963F-404A-AD91-D3F078F825A7 Q38872573-AC49C94E-9490-4A38-8C5C-AD301A4FA23E Q39358889-DAC65DE2-A9F6-409C-9FD4-34D5DBEF4DA0 Q39965786-EDC893E5-D813-4FC8-A88C-E496F26672F2 Q44052705-600DA34D-2A90-4CA9-A66D-D9A972874FBB Q44199828-AD786B9D-2B5C-42F7-8A44-D207521A6A72 Q45417049-B20A8899-5810-41BE-9480-CE3C4F1A6916 Q45876893-1FE48AFE-912F-4085-BE24-A0E16D0C5690 Q46210619-FCAC3772-0EDF-497D-AE75-D1DE8CD807CA Q49418717-233F4A26-99A9-468B-8A2D-A0C3FD19C1AA Q49578189-A9FA5DCF-8E0A-4799-99B5-66C4B7701E01 Q50219536-C495D5D1-57FC-4B77-B042-2ADC743189BB Q51952874-62D73C88-5E9D-44FA-9158-BC9784D45C6B

P2860

Liver transplantation for glycogen storage disease types I, III, and IV

http://www.wikidata.org/entity/Q33797826

description

1999 nî lūn-bûn

@nan

1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1999年の論文

@ja

1999年論文

@yue

1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

name

Liver transplantation for glycogen storage disease types I, III, and IV

@ast

Liver transplantation for glycogen storage disease types I, III, and IV

@en

type

label

Liver transplantation for glycogen storage disease types I, III, and IV

@ast

Liver transplantation for glycogen storage disease types I, III, and IV

@en

prefLabel

Liver transplantation for glycogen storage disease types I, III, and IV

@ast

Liver transplantation for glycogen storage disease types I, III, and IV

@en

P1433

Q33797826-ADAB66EC-24D6-44A2-8E77-85BC36F5177B

P1476

Q33797826-2FF49D92-E2B4-46B7-AB77-63695EB43486

P2093

Q33797826-03AFC2E2-D55E-4F0E-801D-A4B7A97E063F

Q33797826-16AAB911-0C3D-4DE0-A97A-8E620503886C

Q33797826-26CA85F6-946F-4FF3-86CE-0B5C511ECC93

Q33797826-3DE5DDA4-BE45-408B-BEBC-2C7A54B4C870

Q33797826-43B52205-012C-4F2F-9E84-B3E9BC35B89B

Q33797826-51FEB61B-C4BB-49BC-B2C3-A0F9A5161E26

Q33797826-5A3EC883-3387-44A1-9CEE-67B7B4ADAC42

Q33797826-60C2C2C3-7665-473E-B1F4-4F495A988875

Q33797826-88E202F4-C70D-4AD3-8F84-71FE7C2AC893

Q33797826-90474619-A161-43AE-B167-BB20D1EBCFA5

P2860

Q33797826-068AF180-A54C-4967-945A-1D41F5E4E1A6

Q33797826-2AEDC426-564D-44AC-808F-BEC52B447FE6

Q33797826-4832EDE7-15F7-45F3-9DCB-1F0F09BCB589

Q33797826-6F3ABFD1-E39A-418F-9B5D-8E0206542F47

Q33797826-84002B06-BB63-4368-BE9A-A2A0B881E73F

Q33797826-8844DC87-C99B-4A75-AF90-15DBBE97F81E

Q33797826-8873C504-95FC-472C-9A74-692384E6C63F

Q33797826-98D5F8E0-0D03-4957-8A8E-A1D1D4E6B28E

Q33797826-B5CFBDCC-B19D-4E0F-9F89-E7115BA4FD06

Q33797826-CBC3C424-D75D-444E-B29F-42804DB9A80D

P2888

Q33797826-2FB63F6A-E3E4-435E-93A2-F1204A59C39C

P304

Q33797826-03478BC3-11C1-4101-BA8E-46114D0D5C42

P31

Q33797826-10EDFF2C-0CB0-436F-8290-0EA5DAEA2C51

P356

Q33797826-4CFEDB01-DBF1-4A01-94F3-7948E0ADAAB4

P478

Q33797826-5C65A7AF-42EA-49E9-B6E2-E2866769B3AC

P50

Q33797826-92994B70-63F6-44BE-BD05-B356A928CB05

P577

Q33797826-D2670059-9495-45C8-977C-72E540857E42

P6179

Q33797826-1FD2397E-AA88-4331-BB09-FE39CD0A0664

P698

Q33797826-F26D7F4E-9B09-47D1-87C4-798A2658BB62

P921

Q33797826-10229052-6FA3-421C-A4AF-A3E4CDD7A620

P932

Q33797826-D223AC72-8A68-4ED4-8869-CF292FDAA5A6

P356

P1433

European Journal of Pediatrics

P1476

Liver transplantation for glycogen storage disease types I, III, and IV

@en

P2093

A Dhawan

http://www.w3.org/2001/XMLSchema#string

A Lachaux

http://www.w3.org/2001/XMLSchema#string

D Matern

http://www.w3.org/2001/XMLSchema#string

E B Haagsma

http://www.w3.org/2001/XMLSchema#string

G Hug

http://www.w3.org/2001/XMLSchema#string

G P Smit

http://www.w3.org/2001/XMLSchema#string

J Barnard

http://www.w3.org/2001/XMLSchema#string

J Emond

http://www.w3.org/2001/XMLSchema#string

J S Bynon

http://www.w3.org/2001/XMLSchema#string

W Arnaout

http://www.w3.org/2001/XMLSchema#string

P2860

Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene

Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle

Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease

Type I glycogen storage disease: nine years of management with cornstarch.

Liver transplantation for type I and type IV glycogen storage disease.

Liver transplantation for type I glycogen storage disease

Growth in adulthood after liver transplantation for glycogen storage disease type I.

Pathophysiology and dietary treatment of the glycogen storage diseases.

Hepatic adenomata in type Ia glycogen storage disease.

A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.

P2888

P304

S43-8

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/PL00014320

http://www.w3.org/2001/XMLSchema#string

P478

158 Suppl 2

http://www.w3.org/2001/XMLSchema#string

P50

Thomas E. Starzl

P577

1999-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1017206973

http://www.w3.org/2001/XMLSchema#string

P698

10603098

http://www.w3.org/2001/XMLSchema#string

P921

liver transplantation

P932

3006437

http://www.w3.org/2001/XMLSchema#string