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Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti
|
October 20, 2021
BILATERAL AMYLOIDOSIS OF THREE EYELIDS. A CASE REPORT
J Krásný, J Šach, H Hůlková, et al.
Journal of Inherited Metabolic Disease
|
June 27, 2009
Autopsy case of Gaucher disease type I in a patient on enzyme replacement therapy. Comments on the dynamics of persistent storage process
H Hůlková, J Ledvinová, H Poupetová, et al.
Virchows Archiv : an International Journal of Pathology
|
May 27, 2005
Lactosylceramide in lysosomal storage disorders: a comparative immunohistochemical and biochemical study
H Hůlková, J Ledvinová, B Asfaw, et al.
Casopis Lekaru Ceskych
|
April 4, 2000
[Postmortem diagnosis of Fabry disease in a female heterozygote leading to the detection of undiagnosed manifest disease in the family]
H Hůlková, J Ledvinová, H Poupĕtová, et al.
Journal of Inherited Metabolic Disease
|
July 25, 2008
Abnormal expression and processing of uromodulin in Fabry disease reflects tubular cell storage alteration and is reversible by enzyme replacement therapy
P Vylet'al, H Hůlková, M Zivná, et al.
Casopis Lekaru Ceskych
|
April 3, 2002
[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]
M Capková, M Tesarová, L Wenchich, et al.
European Journal of Histochemistry : EJH
|
June 19, 2010
Histochemical detection of GM1 ganglioside using cholera toxin-B subunit. Evaluation of critical factors optimal for in situ detection with special emphasis to acetone pre-extraction
T Petr, V Smíd, J Smídová, et al.
Casopis Lekaru Ceskych
|
September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]
L Stratilová, J Zeman, H Hansíková, et al.
Folia Biologica
|
March 30, 2013
Rapid isolation of lysosomal membranes from cultured cells
D Mušálková, J Lukáš, F Majer, et al.
Casopis Lekaru Ceskych
|
November 24, 1999
[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]
L Stratilová, J Zeman, H Houst'ková, et al.
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
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Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti
|
October 20, 2021
BILATERAL AMYLOIDOSIS OF THREE EYELIDS. A CASE REPORT
J Krásný, J Šach, H Hůlková, et al.
Journal of Inherited Metabolic Disease
|
June 27, 2009
Autopsy case of Gaucher disease type I in a patient on enzyme replacement therapy. Comments on the dynamics of persistent storage process
H Hůlková, J Ledvinová, H Poupetová, et al.
Virchows Archiv : an International Journal of Pathology
|
May 27, 2005
Lactosylceramide in lysosomal storage disorders: a comparative immunohistochemical and biochemical study
H Hůlková, J Ledvinová, B Asfaw, et al.
Casopis Lekaru Ceskych
|
April 4, 2000
[Postmortem diagnosis of Fabry disease in a female heterozygote leading to the detection of undiagnosed manifest disease in the family]
H Hůlková, J Ledvinová, H Poupĕtová, et al.
Journal of Inherited Metabolic Disease
|
July 25, 2008
Abnormal expression and processing of uromodulin in Fabry disease reflects tubular cell storage alteration and is reversible by enzyme replacement therapy
P Vylet'al, H Hůlková, M Zivná, et al.
Casopis Lekaru Ceskych
|
April 3, 2002
[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]
M Capková, M Tesarová, L Wenchich, et al.
European Journal of Histochemistry : EJH
|
June 19, 2010
Histochemical detection of GM1 ganglioside using cholera toxin-B subunit. Evaluation of critical factors optimal for in situ detection with special emphasis to acetone pre-extraction
T Petr, V Smíd, J Smídová, et al.
Casopis Lekaru Ceskych
|
September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]
L Stratilová, J Zeman, H Hansíková, et al.
Folia Biologica
|
March 30, 2013
Rapid isolation of lysosomal membranes from cultured cells
D Mušálková, J Lukáš, F Majer, et al.
Casopis Lekaru Ceskych
|
November 24, 1999
[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]
L Stratilová, J Zeman, H Houst'ková, et al.
Page
of 2