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F Haverkamp

Showing results (51-60 of 65) with videos related to

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Zeitschrift Fur Geburtshilfe Und Neonatologie|January 24, 1998
[Sialidosis and galactosialidosis as the cause of non-immunologic hydrops fetalis]M Schmidt, H Fahnenstich, F Haverkamp, et al.
Fetal Diagnosis and Therapy|March 1, 1996
Nonimmune hydrops fetalis with galactosialidosis: consequences for family planningF Haverkamp, D Jacobs, M Cantz, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|August 1, 1989
[Megacystis microcolon intestinal hypoperistalsis syndrome: A neuropathy?]L Bindl, D Emons, F Haverkamp, et al.
Cureus|July 19, 2023
The Use of Mock Standardized/Simulated Patient Encounters in Facilitating Development of Clinical Competence in Medical StudentsNga N Tran, Denisia Thomas, Chloe F Haverkamp, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Neurodevelopmental outcome after intrauterine red cell transfusion for parvovirus B19-induced fetal hydropsJ Dembinski, F Haverkamp, H Maara, et al.
European Journal of Pediatrics|June 23, 1999
Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counsellingF Haverkamp, J Wölfle, M Aretz, et al.
Acta Endocrinologica|December 1, 1987
Plasma levels of growth hormone-releasing hormone and somatostatin in response to a mixed meal and during sleep in childrenR Rosskamp, M Becker, F Haverkamp, et al.
Klinische Padiatrie|July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]G Schmid, F Haverkamp, J Rechmann, et al.
Klinische Padiatrie|September 1, 1993
[Direct genotype analysis in congenital myotonic dystrophy with an unusual family anamnesis]L Bindl, W Rummel, S Walter, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Zeitschrift Fur Geburtshilfe Und Neonatologie|January 24, 1998
[Sialidosis and galactosialidosis as the cause of non-immunologic hydrops fetalis]M Schmidt, H Fahnenstich, F Haverkamp, et al.
Fetal Diagnosis and Therapy|March 1, 1996
Nonimmune hydrops fetalis with galactosialidosis: consequences for family planningF Haverkamp, D Jacobs, M Cantz, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|August 1, 1989
[Megacystis microcolon intestinal hypoperistalsis syndrome: A neuropathy?]L Bindl, D Emons, F Haverkamp, et al.
Cureus|July 19, 2023
The Use of Mock Standardized/Simulated Patient Encounters in Facilitating Development of Clinical Competence in Medical StudentsNga N Tran, Denisia Thomas, Chloe F Haverkamp, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Neurodevelopmental outcome after intrauterine red cell transfusion for parvovirus B19-induced fetal hydropsJ Dembinski, F Haverkamp, H Maara, et al.
European Journal of Pediatrics|June 23, 1999
Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counsellingF Haverkamp, J Wölfle, M Aretz, et al.
Acta Endocrinologica|December 1, 1987
Plasma levels of growth hormone-releasing hormone and somatostatin in response to a mixed meal and during sleep in childrenR Rosskamp, M Becker, F Haverkamp, et al.
Klinische Padiatrie|July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]G Schmid, F Haverkamp, J Rechmann, et al.
Klinische Padiatrie|September 1, 1993
[Direct genotype analysis in congenital myotonic dystrophy with an unusual family anamnesis]L Bindl, W Rummel, S Walter, et al.
Journal of Medical Genetics|August 3, 2000
Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsyB C Gohlke, K Haug, M Fukami, et al.
Pageof 7