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D Emons

Showing results (21-30 of 34) with videos related to

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Klinische Padiatrie|November 1, 1987
[Idiopathic juvenile osteoporosis--report of 2 cases]R Rosskamp, G Sell, D Emons, et al.
International Journal of Pediatric Otorhinolaryngology|January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstructionF Haverkamp, D Emons, H J Straehler-Pohl, et al.
Klinische Wochenschrift|April 15, 1971
Comparative study of intestinal disaccharidases in Thai and European subjectsH W Rotthauwe, D Emons, M Kaeoplung, et al.
Journal of Medical Genetics|March 1, 1995
Familial schizencephaly: further delineation of a rare disorderF Haverkamp, K Zerres, B Ostertun, et al.
Zeitschrift Fur Urologie Und Nephrologie|March 1, 1988
[Ectopic ureterocele--diagnosis and therapy]H van Ahlen, P Brühl, A Bockisch, et al.
American Journal of Medical Genetics|December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndromeP Rabe, F Haverkamp, D Emons, et al.
Klinische Padiatrie|March 1, 1990
[Schizencephaly]J H Lu, R Mielke, T P Lê, 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.
Klinische Padiatrie|April 24, 2004
Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndromeB Lindenthal, R Repgen, D Emons, et al.
AJNR. American Journal of Neuroradiology|June 1, 1995
Extracerebral intracranial glioneural hamartoma with extension into the parapharyngeal spaceJ D Moritz, D Emons, O D Wiestler, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Klinische Padiatrie|November 1, 1987
[Idiopathic juvenile osteoporosis--report of 2 cases]R Rosskamp, G Sell, D Emons, et al.
International Journal of Pediatric Otorhinolaryngology|January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstructionF Haverkamp, D Emons, H J Straehler-Pohl, et al.
Klinische Wochenschrift|April 15, 1971
Comparative study of intestinal disaccharidases in Thai and European subjectsH W Rotthauwe, D Emons, M Kaeoplung, et al.
Journal of Medical Genetics|March 1, 1995
Familial schizencephaly: further delineation of a rare disorderF Haverkamp, K Zerres, B Ostertun, et al.
Zeitschrift Fur Urologie Und Nephrologie|March 1, 1988
[Ectopic ureterocele--diagnosis and therapy]H van Ahlen, P Brühl, A Bockisch, et al.
American Journal of Medical Genetics|December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndromeP Rabe, F Haverkamp, D Emons, et al.
Klinische Padiatrie|March 1, 1990
[Schizencephaly]J H Lu, R Mielke, T P Lê, 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.
Klinische Padiatrie|April 24, 2004
Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndromeB Lindenthal, R Repgen, D Emons, et al.
AJNR. American Journal of Neuroradiology|June 1, 1995
Extracerebral intracranial glioneural hamartoma with extension into the parapharyngeal spaceJ D Moritz, D Emons, O D Wiestler, et al.
Pageof 4