S. Stöckler‐Ipsiroglu
发表
Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app
C. Ferreira,
C. V. van Karnebeek,
S. Wortmann,
2021,
Orphanet Journal of Rare Diseases.
E. Moser,
F. Ebner,
D. Prayer,
2003,
Neuropediatrics.
S. Stöckler‐Ipsiroglu,
G. Salomons,
S. Mercimek-Mahmutoglu,
2011
.
O. Bodamer,
S. Stockler-Ipsiroglu,
S. Stöckler‐Ipsiroglu,
2003,
Journal of Inherited Metabolic Disease.
O. Bodamer,
O. Bodamer,
S. Stockler-Ipsiroglu,
2005,
Acta paediatrica.
R. Surtees,
O. Bodamer,
S. Stöckler‐Ipsiroglu,
2002,
Clinical chemistry.
A. Fatemi,
S. Stöckler‐Ipsiroglu,
W. Sperl,
2002,
European Journal of Pediatrics.
M. Tosetti,
G. Cioni,
R. Battini,
2002,
Molecular genetics and metabolism.
S. Stöckler‐Ipsiroglu,
O. Ipsiroglu,
H. Höger,
2001,
Life sciences.
S. Stöckler‐Ipsiroglu,
S. Mercimek-Mahmutoglu,
J. Sykut-Cegielska,
2004,
Acta biochimica Polonica.
J. Sass,
S. Stöckler‐Ipsiroglu,
K. Schwab,
2010,
Klinische Ernährungsmedizin.
S. Stöckler‐Ipsiroglu,
A. Schulze,
O. Braissant,
2022,
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases.
A. Beaudet,
W. O'Brien,
F. Scaglia,
2005,
Annals of neurology.
S. Stöckler‐Ipsiroglu,
A. Mühl,
J. Ilas,
2000,
Clinica chimica acta; international journal of clinical chemistry.
R. Battini,
S. Stöckler‐Ipsiroglu,
N. Verhoeven,
2003,
Clinical chemistry.
O. Haas,
S. Stöckler‐Ipsiroglu,
E. Panzer-Grümayer,
2002,
Blood.
S. Stöckler‐Ipsiroglu,
P. Burgard,
H. Bode,
2005,
Wiener klinische Wochenschrift.
S. Stöckler‐Ipsiroglu,
2000
.
S. Stöckler‐Ipsiroglu,
V. Shih,
S. Stöckler‐ipsiroglu,
2000
.
O. Bodamer,
S. Stöckler‐Ipsiroglu,
C. Item,
2005,
Molecular genetics and metabolism.
S. Stöckler‐Ipsiroglu,
S. Greber-Platzer,
C. Item,
2002,
Pediatric Research.
J. Zeman,
J. Zeman,
S. Stöckler‐Ipsiroglu,
2003,
Clinical pediatrics.
C. Spiss,
S. Stöckler‐Ipsiroglu,
J. Zacherl,
2001,
Transplant international : official journal of the European Society for Organ Transplantation.
U. Salzer-Muhar,
S. Stöckler‐Ipsiroglu,
R. Birnbacher,
2003,
Pediatric neurology.
J. Hennig,
T. Thiel,
S. Stöckler‐Ipsiroglu,
2004,
Molecular genetics and metabolism.
Colin A. Johnson,
T. Bourgeron,
K. Lesch,
2009
.
B. Plecko,
S. Stöckler‐Ipsiroglu,
S. Stöckler‐ipsiroglu,
2009,
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques.
H. Mandel,
J. Smeitink,
L. P. Van den Heuvel,
2001,
Annals of neurology.
E. Mariman,
M. Schuelke,
J. Smeitink,
1999,
Nature Genetics.
T. Bourgeron,
J. Sznajder,
E. Viding,
1992,
The British journal of surgery.
A. L. Wong,
J. Belmont,
M. Dichgans,
2011
.
A. L. Wong,
J. Belmont,
D. Roden,
1990,
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.
J. Zeman,
O. Bodamer,
O. Bodamer,
2003
.
B. Plecko,
S. Stöckler‐Ipsiroglu,
C. Jakobs,
2000,
Annals of neurology.
V Wienert,
G Hauer,
A Lentner,
1996,
Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen.
T. Bourgeron,
K. Lesch,
J. Sznajder,
2020,
Definitions.
S. Stöckler‐Ipsiroglu,
M. Huemer,
T. Lang,
2003,
Clinical and experimental rheumatology.
P. Pouwels,
E. Peeters,
M. S. van der Knaap,
2000,
Annals of neurology.
S. Stöckler‐Ipsiroglu,
1997,
The Journal of pediatrics.
Georg Heinze,
Sylvia Stöckler-Ipsiroglu,
G. Heinze,
2007,
Clinical chemistry.
M. Gahr,
F. Hanefeld,
S. Stöckler‐Ipsiroglu,
2000,
Journal of Inherited Metabolic Disease.
E. Viding,
G. Kojda,
M. Digilio,
2020,
Definitions.
S. Lalani,
K. Chayama,
A. Cleare,
2020,
Definitions.
G. Heinze,
F. Waldhauser,
S. Stöckler‐Ipsiroglu,
2002,
Clinical chemistry.
S. Lalani,
K. Chayama,
A. Cleare,
1984,
Current problems in clinical biochemistry.
Colin A. Johnson,
T. Bourgeron,
K. Lesch,
2016
.
F. Waldhauser,
O. Bodamer,
S. Stöckler‐Ipsiroglu,
2007
.
S. Berkovic,
D. Timson,
J. Thoden,
2020,
Definitions.
S. Stöckler‐Ipsiroglu,
S. Mercimek-Mahmutoglu,
W. Gradowska,
2004,
Acta biochimica Polonica.
T. Bourgeron,
E. Viding,
G. Kojda,
2019,
Bailliere's clinical endocrinology and metabolism.
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
S. Lalani,
K. Chayama,
M. Vikkula,
1999,
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
S. Stöckler‐Ipsiroglu,
Olivier Braissant,
Andreas Schulze,
2022,
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases.
Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria.
H. Ulmer,
O. Bodamer,
S. Stöckler‐Ipsiroglu,
2008,
Molecular genetics and metabolism.