W. Sperl
发表
A. Klausegger,
M. Hell,
A. Berger,
1999,
Journal of Clinical Microbiology.
A. Klausegger,
M. Hell,
A. Berger,
1999,
Journal of Clinical Microbiology.
T. Wieland,
T. Meitinger,
T. Strom,
2014,
Molecular genetics and metabolism.
W. Sperl,
B. Kofler,
C. Tuechler,
1998,
Annals of the New York Academy of Sciences.
M. Durán,
D. Lacombe,
J. Sass,
2004,
European Journal of Human Genetics.
C. Fauth,
D. Meierhofer,
J. Zschocke,
2011,
American Journal of Human Genetics.
W. Sperl,
B. Kofler,
J. Mayr,
2017,
Oncotarget.
A. Hermann,
A. Berger,
W. Sperl,
2004,
Endocrinology.
A. Klausegger,
A. Berger,
W. Sperl,
2004,
The Journal of investigative dermatology.
G. Heinze,
O. Bodamer,
W. Sperl,
2006,
Clinica chimica acta; international journal of clinical chemistry.
T. Wieland,
T. Strom,
H. Prokisch,
2017,
European Journal of Human Genetics.
McFarland,
T. Meitinger,
T. Strom,
2016
.
S. Berweck,
M. Staudt,
W. Sperl,
2021,
Neuropediatrics.
S. Kiechl,
W. Sperl,
U. Kohlendorfer,
1998,
American journal of epidemiology.
J. Smeitink,
E. Mayatepek,
E. Morava,
2015,
Journal of Inherited Metabolic Disease.
N. Jones,
W. Sperl,
B. Kofler,
2011,
Frontiers in bioscience.
R. Wanders,
M. Durán,
J. Sass,
2003,
American journal of human genetics.
R. Wanders,
M. Durán,
J. Sass,
2003
.
A. Fatemi,
S. Stöckler‐Ipsiroglu,
W. Sperl,
2002,
European Journal of Pediatrics.
S. Felber,
C. Kremser,
A. Koller,
2000,
Neurological research.
M. Wyss,
S. Felber,
C. Kremser,
1998,
Medical hypotheses.
N. Jones,
W. Sperl,
B. Kofler,
2011,
Frontiers in bioscience.
W. Sperl,
B. Kofler,
F. Rathje,
2018,
Experimental dermatology.
S. Felber,
M. Schocke,
T. Trieb,
2000,
Journal of magnetic resonance imaging : JMRI.
J. Tissot,
W. Sperl,
C. Bachmann,
1997,
The Journal of laboratory and clinical medicine.
Thomas Licht,
Alain Nickels,
G. Rumpold,
2021,
memo - Magazine of European Medical Oncology.
S. Felber,
S. Felber,
W. Sperl,
1993,
Annals of neurology.
J. Sass,
D. Karall,
W. Sperl,
2007,
The Journal of pediatrics.
S. Tims,
T. Coşkun,
Rani H. Singh,
2018,
Expert Opinion on Orphan Drugs.
K. Sargsyan,
W. Sperl,
B. Kofler,
2011,
Frontiers in bioscience.
J. Mair,
B. Puschendorf,
S. Sorichter,
2001,
Clinical chemistry.
W. Sperl,
C. Bachmann,
H. Henry,
1996,
Journal of Inherited Metabolic Disease.
B. Plecko,
M. Huemer,
W. Sperl,
2005,
Archives of Disease in Childhood - Fetal and Neonatal Edition.
C. Heizmann,
N. Blau,
P. Smooker,
1992,
Pediatric Research.
I. Rivera,
H. Prokisch,
R. Rodenburg,
2015,
Journal of Inherited Metabolic Disease.
H. Prokisch,
T. Haack,
W. Sperl,
2016,
Journal of Medical Genetics.
S. Wortmann,
R. Fingerhut,
J. Häberle,
2021,
International journal of neonatal screening.
E. Lamantea,
B. Peterlin,
A. Maver,
2021,
Balkan journal of medical genetics : BJMG.
T. Wieland,
T. Meitinger,
T. Strom,
2012,
Journal of Medical Genetics.
W. Sperl,
B. Kofler,
R. Feichtinger,
2017,
Oncotarget.
Robert W. Taylor,
Alexis A. Jourdain,
V. Mootha,
2017,
American journal of human genetics.
S. Wessler,
T. Cover,
W. Sperl,
2017,
Oxidative medicine and cellular longevity.
A. Trost,
W. Sperl,
B. Kofler,
2016,
Mitochondrion.
B. Plecko,
J. Zschocke,
D. Karall,
2013,
Journal of Inherited Metabolic Disease.
A. Berger,
N. Jones,
W. Sperl,
2005,
Neuropeptides.
A. Berger,
W. Sperl,
B. Kofler,
2002,
Acta Neuropathologica.
W. Schmidt,
W. Sperl,
M. Freilinger,
2022,
Orphanet Journal of Rare Diseases.
A. Berger,
N. Jones,
W. Sperl,
2002,
Neuroendocrinology.
S. Kiechl,
W. Sperl,
U. Kohlendorfer,
1998,
Archives of disease in childhood.
W. Sperl,
E. Ring,
E. Paschke,
1992,
Journal of Inherited Metabolic Disease.
W. Thoenes,
W. Sperl,
F. Fink,
1990,
European Journal of Pediatrics.
T. Suormala,
E. R. Baumgartner,
W. Sperl,
2005,
European Journal of Pediatrics.
M. Baumgartner,
T. Suormala,
S. Grünert,
2012,
Journal of Inherited Metabolic Disease.
M. Baumgartner,
T. Wieland,
T. Meitinger,
2012,
American journal of human genetics.
K. Vesela,
M. Tesařová,
J. Zeman,
2012,
Journal of Inherited Metabolic Disease.
A. Ribes,
P. Briones,
W. Sperl,
2009,
Journal of Inherited Metabolic Disease.
A. Naber,
W. Sperl,
J. Willems,
1997,
Microbial pathogenesis.
M. Hell,
W. Sperl,
B. Kofler,
2007,
Antimicrobial Agents and Chemotherapy.
M. Hell,
W. Sperl,
B. Kofler,
2011,
International Journal of Antimicrobial Agents.
H. Prokisch,
S. Hanein,
A. Rötig,
2018,
American journal of human genetics.
E. Steichen‐Gersdorf,
W. Sperl,
K. Unsinn,
1997,
Clinical dysmorphology.
M. Tarnopolsky,
R. Rodenburg,
M. Knaap,
2012,
Journal of Inherited Metabolic Disease.
T. Meitinger,
H. Prokisch,
T. Haack,
2015,
Journal of Inherited Metabolic Disease.
H. Prokisch,
D. Karall,
W. Sperl,
2011
.
J. Zeman,
J. Houštěk,
W. Sperl,
2002,
Neonatology.
H. Prokisch,
T. Haack,
U. Ahting,
2015,
Orphanet Journal of Rare Diseases.
E. Steichen‐Gersdorf,
W. Sperl,
M. Vanier,
1994,
Journal of Inherited Metabolic Disease.
N. Jones,
W. Sperl,
B. Kofler,
2007,
Journal of Molecular Neuroscience.
R. Wevers,
H. Willems,
W. Sperl,
2000,
Journal of pediatric gastroenterology and nutrition.
M. Widschwendter,
B. Meister,
M. Herold,
1993,
European Journal of Pediatrics.
W. Sperl,
P. Hofbauer,
F. Lagler,
2019,
Archives of Disease in Childhood.
M. Baumgartner,
T. Suormala,
S. Grünert,
2012,
Journal of Inherited Metabolic Disease.
T. Wieland,
A. Munnich,
H. Smeets,
2018
.
B. Koletzko,
W. Sperl,
T. Decsi,
1995,
The American journal of clinical nutrition.
M. Durán,
B. Poll-The,
F. Beemer,
2000,
Journal of Inherited Metabolic Disease.
J. Sass,
Takako Sato,
W. Sperl,
2003,
Biochemical and biophysical research communications.
W. Sperl,
R. Sengers,
J. Guggenbichler,
1990,
European Journal of Pediatrics.
A. Sewell,
W. Sperl,
H. Böhles,
1997,
Journal of Inherited Metabolic Disease.
A. Sewell,
W. Sperl,
H. Böhles,
1997,
The Journal of pediatrics.
Robert W. Taylor,
H. Prokisch,
N. Hauser,
2015,
Journal of Inherited Metabolic Disease.
F. Lindbichler,
C. Mache,
B. Plecko,
2009,
Molecular genetics and metabolism.
H. Prokisch,
R. Rodenburg,
W. Sperl,
2010,
Neuropediatrics.
W. Chan,
H. Prokisch,
F. Alkuraya,
2017,
Human mutation.
T. Meitinger,
T. Strom,
H. Prokisch,
2013,
Journal of Inherited Metabolic Disease.
R. Kaufman,
D. Ginsburg,
Bin Zhang,
2006,
Blood.
W. Sperl,
B. Kofler,
J. Mayr,
2012,
PloS one.
S. Berweck,
M. Staudt,
W. Sperl,
2018,
Neuropediatrics.
M. Zeviani,
D. Neubauer,
M. Meznaric,
2011,
Pediatric neurology.
F. Hanefeld,
C. Binder,
W. Sperl,
1992,
European Journal of Pediatrics.
W. Sperl,
P. Lamparter,
S. Steeb,
2012
.
W. Sperl,
P. Lamparter,
S. Steeb,
1983
.
H. Stuppner,
W. Vogel,
W. Sperl,
1995,
European Journal of Pediatrics.
W. Sperl,
B. Kofler,
J. Bauer,
2014,
Experimental dermatology.
H. Prokisch,
T. Haack,
U. Ahting,
2011,
American journal of human genetics.
J. Sass,
E. Mayatepek,
W. Sperl,
2004,
Clinical pediatrics.
M. Baumgartner,
T. Suormala,
S. Grünert,
2013,
Orphanet Journal of Rare Diseases.
P. Rosenthal,
W. Sperl,
J. Fevery,
1996,
Hepatology.
M. Tesařová,
J. Zeman,
S. Kmoch,
2010,
Archives of Disease in Childhood.
W. Sperl,
U. Wendel,
P. Schadewaldt,
1995,
Journal of Inherited Metabolic Disease.
E. Holme,
J. Zeman,
J. Houštěk,
2006,
Neuromuscular Disorders.
W. Sperl,
B. Kofler,
J. Mayr,
2012,
Biochemical and biophysical research communications.
T. Meitinger,
T. Strom,
H. Prokisch,
2017,
Oxidative medicine and cellular longevity.
M. Baumgartner,
T. Suormala,
P. Chinnery,
2016,
Journal of Inherited Metabolic Disease.
K. Rostásy,
B. Plecko,
D. Karall,
2009,
Neuropediatrics.
Marni J. Falk,
T. Wieland,
T. Meitinger,
2013,
American journal of human genetics.
J. Sass,
W. Sperl,
C. Bachmann,
2001,
The Lancet.
S. Weis,
W. Sperl,
B. Kofler,
2014,
Glia.
T. Wieland,
T. Strom,
H. Prokisch,
2016,
European Journal of Human Genetics.
E. Bertini,
V. Tiranti,
R. Carrozzo,
2019,
The Journal of clinical investigation.
N. Jones,
W. Sperl,
B. Kofler,
2010,
BMC Cancer.
P. Huppke,
M. Schubach,
J. Gärtner,
2015,
Mitochondrion.
W. Sperl,
B. Kofler,
Raphael J. Morscher,
2016,
Oncotarget.
W. Sperl,
B. Kofler,
R. Feichtinger,
2015,
Translational pediatrics.
W. Sperl,
S. Reuter,
S. Zierz,
2004,
Mitochondrion.
J. R. Contreras,
Nicole A Weigand,
Colin G Fink,
2019,
Scientific Reports.
W. Sperl,
D. Weghuber,
F. Zimmermann,
2022,
Inflammatory bowel diseases.
D. Meierhofer,
W. Sperl,
B. Kofler,
2008,
Clinical Cancer Research.
W. Sperl,
B. Kofler,
R. Feichtinger,
2015,
The international journal of biochemistry & cell biology.
Sophia Hsin-Jung Li,
J. Rabinowitz,
Zemer Gitai,
2018,
Nature.
J. Zeman,
J. Zeman,
S. Stöckler‐Ipsiroglu,
2003,
Clinical pediatrics.
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism
D. Meierhofer,
W. Sperl,
B. Kofler,
2006,
British Journal of Cancer.
W. Sperl,
B. Kofler,
D. Neureiter,
2015,
PloS one.
D. Meierhofer,
A. Berger,
W. Sperl,
2004,
Carcinogenesis.
S. Seneca,
P. Divina,
M. Tesařová,
2012
.
S. Wortmann,
W. Sperl,
D. Weghuber,
2020,
Acta paediatrica.
S. Weis,
W. Sperl,
B. Kofler,
2016,
Neuro-oncology.
W. Sperl,
B. Kofler,
C. Grethen,
2001,
Diagnostic molecular pathology : the American journal of surgical pathology, part B.
Alexander Hoischen,
Arnold Munnich,
Ron A Wevers,
2018,
American journal of human genetics.
W. Sperl,
R. Sengers,
J. Guggenbichler,
1988,
European Journal of Pediatrics.
H. Holzmann,
N. Jones,
W. Sperl,
2007,
The Pediatric infectious disease journal.
Robert W. Taylor,
Vicente A. Yépez,
J. Gagneur,
2021,
medRxiv.
Robert W. Taylor,
Courtney E. French,
A. Pagnamenta,
2018,
American Journal of Human Genetics.
H. Prokisch,
S. Wortmann,
W. Sperl,
2017,
Neuropediatrics.
S. Kohlwein,
Hanns Lochmüller,
R. Horvath,
2007,
American journal of human genetics.
R. Horvath,
B. Schoser,
B. Czermin,
2011,
Neuromuscular Disorders.
C. Fauth,
J. Zschocke,
W. Sperl,
2012,
Neuropediatrics.
J. Houštěk,
W. Sperl,
P. Pecina,
2004,
Pediatric Research.
W. Sperl,
R. Sengers,
W. Ruitenbeek,
1993,
Enzyme & protein.
W. Sperl,
C. Chéry,
F. Namour,
2011,
Haematologica.
W. Sperl,
C. Chéry,
F. Namour,
2011
.
Robert W. Taylor,
W. Chung,
H. Prokisch,
2017,
Annals of neurology.
Colin A. Johnson,
E. R. Baumgartner,
T. Meitinger,
2016,
American journal of human genetics.
W. Wurst,
H. Prokisch,
M. D. de Angelis,
2015,
Human molecular genetics.
K. Hejzlarová,
M. Tesařová,
M. Vrbacký,
2008,
Nature Genetics.
V. Kaplanová,
V. Havlíčková,
J. Houštěk,
2010,
Human molecular genetics.
Robert W. Taylor,
T. Meitinger,
S. Seneca,
2015,
Front. Genet..
F. Tort,
A. Ribes,
W. Sperl,
2014,
Journal of Inherited Metabolic Disease.
W. Sperl,
2011
.
M. Widschwendter,
B. Meister,
M. Tötsch,
1994,
Biology of the neonate.
H. Prokisch,
W. Yue,
S. Banka,
2014,
Molecular genetics and metabolism.
H. Klocker,
B. Paulweber,
W. Horninger,
2009,
PloS one.
C. Datz,
B. Paulweber,
M. Halle,
2015,
PloS one.
W. Sperl,
B. Kofler,
D. Neureiter,
2022,
Oxidative Medicine and Cellular Longevity.
J. R. Contreras,
Nicole A Weigand,
Colin G Fink,
2022,
European Journal of Pediatrics.
H. Prokisch,
U. Löbel,
T. Haack,
2017,
Mitochondrion.
D. Meierhofer,
W. Sperl,
B. Kofler,
2005,
Mitochondrion.
J. Léger,
M. Cremer,
W. Kress,
1995,
Neuromuscular Disorders.
B. Alinger,
W. Eder,
N. Jones,
2009,
British Journal of Cancer.
S. Kiechl,
J. Willeit,
K. Gempel,
2002,
Journal of Inherited Metabolic Disease.
F. Waldhauser,
O. Bodamer,
W. Sperl,
2006,
European Journal of Pediatrics.
F. Hanefeld,
W. Sperl,
R. Sengers,
1990,
European Journal of Pediatrics.
S. Kiechl,
W. Oberaigner,
U. P. Peglow,
2001,
Wiener Klinische Wochenschrift.
W. Sperl,
J. Wayenberg,
1992,
European Journal of Pediatrics.
W. Sperl,
B. Schellmann,
1979,
Zeitschrift fur Rechtsmedizin. Journal of legal medicine.
W. Sperl,
W. Lehnert,
1990,
Klinische Padiatrie.
M. Wyss,
W. Sperl,
F. Gellerich,
1997,
Molecular and Cellular Biochemistry.
Robert W. Taylor,
R. Durbin,
T. Wieland,
2015,
Annals of clinical and translational neurology.
F. Berthold,
N. Jones,
W. Sperl,
2011,
Frontiers in bioscience.
T. Suormala,
J. Sass,
W. Sperl,
2000,
European Journal of Pediatrics.
W. Sperl,
B. Kofler,
D. Weghuber,
2020,
Oxidative medicine and cellular longevity.
R. Płoski,
M. Pronicki,
J. Książyk,
2016,
Molecular genetics and metabolism reports.
Robert W. Taylor,
T. Meitinger,
S. Seneca,
2017
.
M. Durán,
R. Wevers,
S. Wortmann,
2013,
Journal of Inherited Metabolic Disease.
E. Boltshauser,
W. Sperl,
H. Strassburg,
2006,
Neuropediatrics.
W. Eder,
W. Sperl,
B. Kofler,
2012,
PloS one.
W. Sperl,
P. Lamparter,
S. Steeb,
2013
.
W. Sperl,
P. Lamparter,
S. Steeb,
1982
.
W. Sperl,
P. Lamparter,
S. Steeb,
1981
.
C. Fauth,
D. Karall,
W. Sperl,
2018,
Congenital heart disease.
B. Paulweber,
W. Renner,
M. Weger,
2009,
BMC Medical Genetics.
E. Bertini,
H. Mandel,
S. Rahman,
2015,
Journal of Inherited Metabolic Disease.
W. Sperl,
1997,
Wiener Klinische Wochenschrift.
H. Prokisch,
T. Haack,
O. Bodamer,
2011,
Molecular genetics and metabolism.
G. Pruijn,
J. Veltman,
H. Prokisch,
2017,
Human mutation.
R. Wevers,
J. Smeitink,
W. Sperl,
1992,
Annals of clinical biochemistry.
J. Zeman,
J. Houštěk,
W. Sperl,
2005
.
T. Meitinger,
V. Tiranti,
M. Zeviani,
2011,
Journal of Medical Genetics.
W. Sperl,
B. Kofler,
D. Neureiter,
2018,
Cells.
S. Wortmann,
W. Sperl,
J. Mayr,
2020,
Journal of mother and child.
W. Sperl,
W. Doesburg,
J. Boon,
1992,
Annals of clinical biochemistry.
W. Sperl,
R. Sengers,
G. Korenke,
1990,
Journal of Inherited Metabolic Disease.
Ž. Reiner,
W. Sperl,
Zoran Mitrović,
2012,
European Journal of Human Genetics.
W. Sperl,
Zoran Mitrović,
I. Barić,
2013
.
R. Wanders,
M. Durán,
J. Sass,
2003
.
H. Budka,
M. Huemer,
D. Meierhofer,
2003,
Acta Neuropathologica.
Robert W. Taylor,
T. Wieland,
A. Munnich,
2018,
Orphanet Journal of Rare Diseases.
C. Pérez-Cerdá,
J. Sass,
M. Ugarte,
1999,
Human mutation.
D. Meierhofer,
N. Jones,
W. Sperl,
2006,
Leukemia.
T. Meitinger,
T. Strom,
H. Prokisch,
2017,
Brain : a journal of neurology.
B. Plecko,
D. Karall,
W. Sperl,
2015,
Orphanet Journal of Rare Diseases.
W. Sperl,
F. Gellerich,
E. Gnaiger,
1994,
Journal of Inherited Metabolic Disease.
J. Reiss,
J. Sass,
W. Sperl,
2003,
Journal of Inherited Metabolic Disease.
B. Paulweber,
W. Eder,
W. Sperl,
2011,
PloS one.
B. Paulweber,
B. Iglseder,
W. Eder,
2011,
PloS one.
E. Steichen‐Gersdorf,
W. Sperl,
C. Murr,
1992,
Journal of Inherited Metabolic Disease.
W. Sperl,
J. Guggenbichler,
R. Geiger,
1990,
The Lancet.
W. Sperl,
B. Simma,
I. Hammerer,
1990,
Klinische Pädiatrie.
Fulminant hepatic failure in a child as a potential adverse effect of trimethoprim-sulphamethoxazole
B. Meister,
F. Fend,
R. Margreiter,
1995,
European Journal of Pediatrics.
W. Sperl,
R. Sengers,
W. Ruitenbeek,
1992,
Neuromuscular Disorders.
W. Sperl,
J. Guggenbichler,
J. Parth,
1986,
Padiatrie und Padologie.
S. Seneca,
P. Divina,
M. Tesařová,
2008,
BMC Genomics.
B. Meister,
M. Tötsch,
W. Sperl,
1992,
The Lancet.
W. Elliott,
W. Sperl,
G. Weber,
1988,
Padiatrie und Padologie.
R. Horvath,
J. Gärtner,
W. Sperl,
2014,
Neuromuscular Disorders.
J. Sass,
W. Sperl,
Jörn Oliver Sass,
2004,
Brain and Development.
W. Sperl,
A. Doronjski,
V. Stojanović,
2013,
Croatian medical journal.
W. Sperl,
R. Sengers,
J. Guggenbichler,
1990,
European Journal of Pediatrics.
Yeast mediates lactic acidosis suppression after antibiotic cocktail treatment in short small bowel?
W. Sperl,
G. Bongaerts,
R. Severijnen,
2005,
Scandinavian journal of gastroenterology.
B. Ertl-Wagner,
H. Bolz,
E. Boltshauser,
2016,
European journal of medical genetics.
J. Ehrich,
M. Pettoello‐Mantovani,
W. Sperl,
2016,
The Journal of pediatrics.
G. Ladurner,
E. Trinka,
W. Sperl,
2001,
Epilepsia.
C. Humpel,
M. Huemer,
A. Berger,
2003,
Acta Neuropathologica.
B. Paulweber,
D. Meierhofer,
W. Sperl,
2006,
Electrophoresis.
T. Meitinger,
H. Prokisch,
T. Haack,
2013
.
M. Baumgartner,
T. Wieland,
T. Meitinger,
2012,
American journal of human genetics.
M. Hell,
W. Sperl,
B. Kofler,
2011,
International journal of antimicrobial agents.
C. Fauth,
D. Meierhofer,
J. Zschocke,
2011,
American journal of human genetics.
W. Sperl,
R. Geiger,
Willy Lehnert,
1997,
European Journal of Pediatrics.
W. Sperl,
J. Colombo,
E. Plöchl,
1996,
Klinische Padiatrie.
John Herbert,
Francesca M. Buffa,
Henrik Vorschmitt,
2008
.
R. Kaufman,
D. Ginsburg,
Bin Zhang,
2006,
Blood.
T. Wieland,
T. Meitinger,
T. Strom,
2014,
Molecular genetics and metabolism.
W. Sperl,
O. Rittinger,
Raphael J. Morscher,
2017,
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