M. Beck
发表
F. Krummenauer,
A. Kohlschütter,
F. Baehner,
2005,
Journal of Inherited Metabolic Disease.
H. Kresse,
A. Tylki-Szymańska,
A. Gal,
1996,
American journal of human genetics.
R. Schiffmann,
P. Elliott,
A. Mehta,
2009,
The Lancet.
A. Schwarting,
F. Krummenauer,
A. Gal,
2004,
Clinical genetics.
A. Mehta,
A. Linhart,
G. Sunder-Plassmann,
2004,
European journal of clinical investigation.
J. Kriegsmann,
B. Winchester,
A. Gal,
2001,
Journal of Inherited Metabolic Disease.
D. Hughes,
P. Deegan,
M. Beck,
2005,
Journal of Medical Genetics.
A. Mehta,
A. Schwarting,
M. Beck,
2003,
Acta paediatrica (Oslo, Norway : 1992). Supplement.
M. Lentze,
M. Beck,
G. Zelczak,
2000,
Acta paediatrica.
H. Trübel,
M. Knuf,
F. Baehner,
2005,
Acta paediatrica (Oslo, Norway : 1992). Supplement.
E. Miebach,
C. Whybra,
M. Beck,
2002,
Acta paediatrica (Oslo, Norway : 1992). Supplement.
S. Feriozzi,
A. Mehta,
A. Schwarting,
2006,
Clinical nephrology.
R. Schiffmann,
P. Elliott,
J. Moon,
2021,
Molecular genetics and metabolism.
A. Mehta,
G. Sunder-Plassmann,
D. Hajioff,
2006,
European journal of clinical investigation.
Z. Lukacs,
E. Mengel,
R. Hartung,
2007,
Journal of Inherited Metabolic Disease.
C. Whybra,
M. Beck,
C. Kampmann,
2013,
Clinical genetics.
T. Maisonobe,
R. Jaussaud,
A. Mehta,
2006,
International journal of clinical practice.
E. Schwinger,
J. Hopwood,
A. Gal,
1993,
Human mutation.
R. Schiffmann,
P. Elliott,
A. Mehta,
2010,
The Lancet.
G. Gildengorin,
R. Giugliani,
J. E. Wraith,
2012,
Journal of Inherited Metabolic Disease.
M. Schlander,
M. Beck,
2009,
Current medical research and opinion.
M. Schlander,
M. Beck,
2009
.
W. Arts,
A. Covanis,
E. Zammarchi,
2000,
Human molecular genetics.
P. Elliott,
A. Mehta,
R. Giugliani,
2009,
Journal of Medical Genetics.
C. Whybra,
C. Kampmann,
M. Beck,
2005,
Journal of Inherited Metabolic Disease.
C. P. Morris,
H. Scott,
E. Schwinger,
1994,
Human molecular genetics.
C. P. Morris,
E. Schwinger,
J. Hopwood,
1993,
Human molecular genetics.
B. Zabel,
E. Schwinger,
J. Hopwood,
1992,
American journal of medical genetics.
E. Schwinger,
J. Hopwood,
A. Gal,
1992,
Human molecular genetics.
C. P. Morris,
A. Sewell,
E. Schwinger,
1992,
Journal of Inherited Metabolic Disease.
A. Mehta,
G. Sunder-Plassmann,
S. Hegemann,
2006,
European journal of clinical investigation.
E. Schwinger,
W. Kleijer,
A. Gal,
1995,
Human mutation.
M. Lentze,
N. Liappis,
M. Beck,
2001,
Clinical chemistry.
H. Runz,
E. Mengel,
R. Hartung,
2011
.
A. Mehta,
A. García de Lorenzo,
M. Beck,
2005,
Journal of Medical Genetics.
A. Gal,
E. Schaefer,
C. Kampmann,
2008,
Journal of Inherited Metabolic Disease.
Enzyme replacement therapy in heterozygous females with Fabry disease: Results of a phase IIIB study
F. Baehner,
E. Miebach,
C. Whybra,
2003,
Journal of Inherited Metabolic Disease.
G. Houge,
A. Mehta,
U. Ramaswami,
2004,
European journal of clinical investigation.
A. Rolfs,
H. Neumann,
M. Beck,
2008,
Deutsche medizinische Wochenschrift.
J. E. Wraith,
M. Beck,
M. Beck,
2010,
Journal of Inherited Metabolic Disease.
G. Kutschke,
F. Birklein,
F. Krummenauer,
2003,
Journal of Inherited Metabolic Disease.
A. Rolfs,
F. Eyskens,
A. Mehta,
2010,
QJM : monthly journal of the Association of Physicians.
R. Jaussaud,
U. Ramaswami,
G. Pintos-Morell,
2007,
The British journal of dermatology.
M. Beck,
M. Beck,
J. Glössl,
1986,
Clinical genetics.
U. Ramaswami,
G. Pintos-Morell,
R. Parini,
2007,
Acta paediatrica.
G. Andria,
J. M. Aerts,
B. Bembi,
2003,
Journal of Inherited Metabolic Disease.