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Carsten G. Bonnemann
Assistant Professor of Neurology
Department: Neurology
Contact information
The Children’s Hospital of Philadelphia
34th & Civic Center Boulevard
Abramson Research Center, #516 A
Philadelphia, PA 19104
34th & Civic Center Boulevard
Abramson Research Center, #516 A
Philadelphia, PA 19104
Office: 2155907490
Graduate Group Affiliations
Education
Graduation from medical school Staatsexamen) with distinction ("sehr gut"). , 1988.
MD
Medical school at Albert-Ludwigs University Freiburg, Germany, 1988.
Doctor of Medicine, "Summa cum laude"., 1989.
“Habilitation” in Pediatrics, University of Göttingen , 2001.
Graduation from medical school Staatsexamen) with distinction ("sehr gut"). , 1988.
MD
Medical school at Albert-Ludwigs University Freiburg, Germany, 1988.
Doctor of Medicine, "Summa cum laude"., 1989.
“Habilitation” in Pediatrics, University of Göttingen , 2001.
Post-Graduate Training
Subinternship (final year of medical school) in medicine and surgery , University Hospital Freiburg, and in neurology at National Hospital for Nervous Diseases, Queen Squa, 1988-.
Clinical fellow in neurology (neuromuscular) and research fellow in genetics , Children’s Hospital/Harvard Medical School. , 1995-1998.
Residency in neurology/child neurology , Massachusetts General Hospital/Harvard Medical School, Boston., 1992-1995.
Resident in Pediatrics and Fellow in Pediatric Neurology, University of Göttingen, Germany., 1998-1999.
Clerkships in radiology and ob/gyn in Essen, Germany; in medicine and surgery , Dublin, Ireland; and in child neurology at Massachusetts General Hospital, Boston. , 1985-1987.
Internship and start of residency , Children's Hospital of Altona, Hamburg, Germany. Training in general pediatrics, neonatology and wor, 1989-1991.
Subinternship (final year of medical school) in medicine and surgery , University Hospital Freiburg, and in neurology at National Hospital for Nervous Diseases, Queen Squa, 1988-.
Clinical fellow in neurology (neuromuscular) and research fellow in genetics , Children’s Hospital/Harvard Medical School. , 1995-1998.
Residency in neurology/child neurology , Massachusetts General Hospital/Harvard Medical School, Boston., 1992-1995.
Resident in Pediatrics and Fellow in Pediatric Neurology, University of Göttingen, Germany., 1998-1999.
Clerkships in radiology and ob/gyn in Essen, Germany; in medicine and surgery , Dublin, Ireland; and in child neurology at Massachusetts General Hospital, Boston. , 1985-1987.
Internship and start of residency , Children's Hospital of Altona, Hamburg, Germany. Training in general pediatrics, neonatology and wor, 1989-1991.
Certifications
Board certification in Pediatrics (Germany) , 2000.
Permanent linkBoard certification in Pediatrics (Germany) , 2000.
Selected Publications
J. Kirschner, I. Hausser, G. Schreiber, H.-J. Christen, S. Brown, I. Anton-Lamprecht, F. Muntoni, F. Hanefeld, C.G. Bönnemann: Ullrich congenital muscular dystrophy: Ultrastructural abnormalities of skin biopsies resemble Ehlers-Danlos syndrome. Submitted 2003.C.G. Bönnemann, K. Brockmann, F. Hanefeld: Muscle ultrasound in Bethlem myopathy. Submitted 2003.
D.G. Sudano, T.C. Pan, R.Z. Zhang, S.K. Marie, U. Wever, M.L. Chu, C.G. Bönnemann: Loss of connection to the basal lamina as a hallmark in collagen type VI related muscular dystrophy. Submitted 2003.
T.C. Pan, R.Z. Zhang, D.G. Sudano, S.K. Marie, C.G. Bönnemann, M.L. Chu: New molecular mechanism for Ullrich congenital muscular dystrophy: A heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. Am J Hum Genet, in press 2003.
C.G. Bönnemann, T.G. Thompson, P.F.M. v.d. Ven, H.H. Goebel, I. Warlo, B. Vollmers, J. Reimann, J. Herms, M. Gautel, F. Takada, A.H. Beggs, D.O. Fürst, L.M. Kunkel, F. Hanefeld, R. Schröder: Filamin C accumulation together with ƒÑB-crystallin is a strong but nonspecific immunohistochemical marker of core formation in muscle. J Neurol Sci 206: 71-78, 2003.
J. Kirschner and C.G. Bönnemann: The congenital and limb girdle muscular dystrophies: Sharpening the focus, blurring the bounderies, forthcoming 2003.
C.G. Bönnemann and K.M.D. Bushby: The limb girdle muscular dystrophies. In: A. Engel and C. Franzini-Armstrong: Myology, 3rd edition, forthcoming 2003.
C.G. Bönnemann: The limb girdle muscular dystrophies. Neuromuscular Disorders of Infancy and Childhood: A Clinician’s Approach. Butterworth-Heinemann, Woburn. H. Royden Jones, Jr, D.C. De Vivo, B.T. Darras (eds.). 2003.
Gussoni, R.R. Bennet, K.R. Muskiewicz, T. Meyerrose, J.A. Nolta, I. Gilgoff, J. Stein, Y. Chan, H.G. Lidov, C.G. Bönnemann, A.v. Moers, G.E. Morris, J.d. Dunnen, J.S. Chamberlain, L.M. Kunkel, K. Weinberg: Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation. J. Clin Invest 110: 807-814, 2002.
A. Ferreiro, B. Estournet, S. Quijano-Roy, B. Moghadazadeh, C. Pichereau, N. Goemans, , C. Bönnemann, H. Jungbluth, V. Straub, M. Villanova, J.-P. Leray, N.B. Romero, J.-J. Martin, F. Muntoni, T. Voit, M. Faredeau, P. Guicheney: Mutations of SEPN1, implicated in rigid spine muscular dystrophy, cause the classical phenotype of multi-minicore disease. Am J Hum Genet 71: 739-749, 2002.
