H. Poupětová
发表
J. Cooper,
R. Giugliani,
Z. Lukacs,
2016,
Molecular genetics and metabolism.
M. Aschermann,
J. Zeman,
A. Linhart,
2000,
American heart journal.
K. Vesela,
M. Tesařová,
J. Zeman,
2009,
Biologia.
D. Maixnerova,
V. Tesar,
J. Reiterová,
2013,
BMC Nephrology.
A. Linhart,
A. Tomek,
M. Vaněčková,
2021,
Journal of clinical medicine.
M. Jirsa,
M. Vanier,
M. Hřebíček,
2019,
Orphanet Journal of Rare Diseases.
F. Tureček,
H. Poupětová,
B. Asfaw,
2013,
Clinica chimica acta; international journal of clinical chemistry.
D. Maixnerova,
V. Tesar,
J. Reiterová,
2006,
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
K. Hodaňová,
H. Hartmannová,
S. Kmoch,
2022,
bioRxiv.
J. Zeman,
M. Elleder,
H. Hulkova,
1999,
Casopis lekaru ceskych.
A. Pshezhetsky,
R. Froissart,
M. Zabot,
2003,
Human mutation.
M. Elleder,
V. Kožich,
H. Poupětová,
1998,
Ceskoslovenska patologie.
M. Elleder,
H. Hulkova,
H. Poupětová,
2009,
Journal of Inherited Metabolic Disease.
A. Lugowska,
J. Sikora,
H. Jahnová,
2017,
Analytical biochemistry.
J. Zeman,
M. Elleder,
H. Poupětová,
2001,
Virchows Archiv.
R. Mazanec,
H. Vlaskova,
Z. Mušová,
2019,
Journal of Neurology.
M. Píšacka,
M. Elleder,
H. Poupětová,
1997,
Biochimica et biophysica acta.
M. Elleder,
M. Hřebíček,
L. Dvořáková,
2005,
American journal of medical genetics. Part A.
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.
P. Mistry,
M. Elleder,
J. Aerts,
2010,
Journal of Inherited Metabolic Disease.
A. Pshezhetsky,
R. Froissart,
M. Zabot,
2003
.
M. Elleder,
H. Poupětová,
K. Harzer,
1994,
Journal of Inherited Metabolic Disease.
M. Elleder,
H. Hulkova,
J. Sikora,
2008,
Virchows Archiv.
A. Linhart,
L. Dvořáková,
G. Dostálová,
2022,
American journal of medical genetics. Part A.
M. Elleder,
V. Kožich,
L. Dvořáková,
2010,
Journal of Inherited Metabolic Disease.
M. Hřebíček,
L. Dvořáková,
H. Vlaskova,
2014,
Orphanet Journal of Rare Diseases.
P. Kuchynka,
A. Linhart,
H. Vlaskova,
2014,
Journal of Inherited Metabolic Disease.
R. Druga,
M. Elleder,
L. Dvořáková,
2008,
Acta Neuropathologica.
M. Elleder,
M. Hřebíček,
H. Hulkova,
2001,
Human molecular genetics.
T. Hudson,
A. Verner,
A. Pshezhetsky,
2006,
American journal of human genetics.
J. Zeman,
M. Elleder,
H. Poupětová,
2001,
Virchows Archiv.
A. Hlavatá,
J. Zeman,
E. Hrubá,
2017,
Clinical genetics.
A. Chlumská,
S. Maas,
M. Elleder,
2000,
Journal of hepatology.
Jana Uřinovská,
M. Hřebíček,
F. Majer,
2010,
Molecular and Cellular Biochemistry.
M. Hřebíček,
J. Sikora,
H. Poupětová,
2005,
BMC Cell Biology.
A. Hlavatá,
J. Zeman,
C. Beesley,
2009,
American journal of medical genetics. Part A.
V. Gieselmann,
M. Elleder,
M. Hřebíček,
2004,
American journal of medical genetics. Part A.
Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiency.
H. Simmonds,
J. Tischfield,
J. Zeman,
1999,
Molecular genetics and metabolism.
J. Zeman,
A. Linhart,
H. Vlaskova,
2018,
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.
J. Zeman,
L. Dvořáková,
H. Poupětová,
2009,
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.
G. Dostálová,
H. Poupětová,
B. Asfaw,
2024,
Clinica chimica acta; international journal of clinical chemistry.
L. Dvořáková,
H. Poupětová,
V. Malinová,
2023,
International journal of molecular sciences.