J. Ledvinová
发表
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Virchows Archiv.
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Analytical biochemistry.
J. Ledvinová,
2020
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M. Jirsa,
M. Vanier,
M. Hřebíček,
2019,
Orphanet Journal of Rare Diseases.
M. Elleder,
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Virchows Archiv A.
F. Tureček,
H. Poupětová,
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Clinica chimica acta; international journal of clinical chemistry.
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J. Ledvinová,
1990,
European journal of biochemistry.
M. Aschermann,
A. Linhart,
M. Elleder,
2001,
Journal of Inherited Metabolic Disease.
D. Maixnerova,
V. Tesar,
J. Reiterová,
2006,
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
M. Elleder,
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2005,
Journal of Molecular Medicine.
J. Zeman,
M. Elleder,
H. Hulkova,
1999,
Casopis lekaru ceskych.
M. Elleder,
H. Hulkova,
F. Šmíd,
2012,
Glycobiology.
M. Hřebíček,
J. Ledvinová,
2010
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M. Hřebíček,
F. Majer,
B. Asfaw,
2022,
Journal of inherited metabolic disease.
M. Elleder,
H. Hulkova,
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Journal of Inherited Metabolic Disease.
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Analytical biochemistry.
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Acta Neuropathologica.
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M. Elleder,
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Virchows Archiv.
D. Schindler,
E. Conzelmann,
B. Černý,
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Journal of lipid research.
M. Aschermann,
J. Zeman,
A. Linhart,
2000,
American heart journal.
R. Desnick,
D. Schindler,
A. Chabás,
2002,
Journal of Lipid Research.
M. Píšacka,
M. Elleder,
H. Poupětová,
1997,
Biochimica et biophysica acta.
M. Elleder,
M. Hřebíček,
L. Dvořáková,
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American journal of medical genetics. Part A.
K. Hodaňová,
J. Zeman,
M. Elleder,
1996,
Virchows Archiv.
C. Michalec,
V. Bradová,
F. Šmíd,
1990,
Journal of chromatography.
Mucolipidosis IV: report of a case with ocular restricted phenotype caused by leaky splice mutation.
K. Jirsova,
M. Elleder,
P. Lišková,
2007,
American journal of ophthalmology.
B. Asfaw,
J. Ledvinová,
L. Kuchař,
2012
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Lauren C. Boudewyn,
S. Walkley,
K. Dobrenis,
2017,
Neurobiology of Disease.
M. Elleder,
H. Poupětová,
K. Harzer,
1994,
Journal of Inherited Metabolic Disease.
Martin Strohalm,
V. Havlíček,
R. Desnick,
2015,
Analytical and Bioanalytical Chemistry.
I. Krägeloh-Mann,
M. Staudt,
M. Elleder,
2009,
American journal of medical genetics. Part A.
M. Elleder,
H. Hulkova,
J. Sikora,
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Virchows Archiv.
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V. Kožich,
L. Dvořáková,
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Journal of Inherited Metabolic Disease.
M. Elleder,
M. Hřebíček,
H. Hulkova,
2001,
Human molecular genetics.
R. Santer,
O. Diggelen,
E. Mengel,
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Journal of Inherited Metabolic Disease.
M. Elleder,
J. Ledvinová,
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Sbornik lekarsky.
J. Zeman,
M. Elleder,
H. Poupětová,
2001,
Virchows Archiv.
H. Mandel,
A. Reuser,
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Molecular genetics and metabolism.
J. Zeman,
M. Hřebíček,
L. Dvořáková,
2016,
Folia biologica.
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S. Maas,
M. Elleder,
2000,
Journal of hepatology.
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M. Elleder,
J. Ledvinová,
2000,
Virchows Archiv.
M. Elleder,
P. Cieslar,
R. Kuhn,
1990,
Virchows Archiv A.
Jana Uřinovská,
M. Hřebíček,
F. Majer,
2010,
Molecular and Cellular Biochemistry.
M. Hřebíček,
J. Sikora,
H. Poupětová,
2005,
BMC Cell Biology.
J. Rybova,
B. Asfaw,
J. Ledvinová,
2016,
Advances in clinical chemistry.
V. Gieselmann,
M. Elleder,
M. Hřebíček,
2004,
American journal of medical genetics. Part A.
J. Zeman,
M. Elleder,
D. Stejskal,
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Ultrastructural pathology.
Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiency.
H. Simmonds,
J. Tischfield,
J. Zeman,
1999,
Molecular genetics and metabolism.
U. Ramaswami,
B. Plecko,
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2009,
Human mutation.
J. Zeman,
K. Sandhoff,
M. Elleder,
2005,
Journal of Inherited Metabolic Disease.
V. Havlíček,
Ľ. Škultéty,
H. Hulkova,
2018,
Glycobiology.
M. Elleder,
H. Rosewich,
M. Hřebíček,
2005,
Neuropediatrics.
J. Sikora,
J. Rybova,
J. Ledvinová,
2018,
Journal of Inherited Metabolic Disease.
Z. Bílková,
L. Korecká,
D. Horák,
2010,
Rapid communications in mass spectrometry : RCM.
B. Plecko,
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E. Paschke,
2008
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