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F Haverkamp

Showing results (31-40 of 65) with videos related to

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Klinische Padiatrie|May 1, 1996
[X-chromosomal recessive hydrocephalus internus: a separate disease picture? 2 further case reports and review of the literature]F Haverkamp, A Krämer, H Fahnenstich, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|July 30, 2013
Initial knowledge at radiation protection courses from 2005-2013 (3): tendencies and conclusionsU F Haverkamp, B A Pruemer, A Fahrmer
European Journal of Pediatrics|December 3, 1998
False-positive serological tests for Lyme disease in facial palsy and varicella zoster meningo-encephalitisJ Woelfle, B Wilske, F Haverkamp, et al.
Klinische Padiatrie|January 31, 1998
[Mitochondrial diseases]J D Nagel, F Haverkamp, M J Lentze
European Journal of Ophthalmology|October 28, 2004
Intraocular pressure, safety and quality of life in glaucoma patients switching to latanoprost from adjunctive and monotherapy treatmentsF Haverkamp, S Wuensch, M Fuchs, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 25, 2000
Symptomatic versus substitution growth hormone therapy in short children: from auxology towards a comprehensive multidimensional assessment of short stature and related interventionsF Haverkamp, U Eiholzer, M B Ranke, et al.
Klinische Padiatrie|October 26, 2000
[Processes of body perception and their therapeutic use in pediatrics. From nonspecific relaxation therapy to training to recognize disease-specific symptoms]M Noeker, U von Rüden, D Staab, et al.
Klinische Padiatrie|January 30, 2004
[Methodological perspectives for the assessment of adaptation in chronic diseases, exemplified by asthma bronchiale in childhood]F Haverkamp, D Staab, K Müller-Sinik, et al.
Clinical Genetics|June 2, 2007
Isolated cystinuria (OMIM 238200) is not a separate entity but is caused by a mutation in the cystinuria gene SLC7A9T Eggermann, M Elbracht, F Haverkamp, et al.
Klinische Padiatrie|November 1, 1990
[7-week-old infant with a hydrolethalus syndrome: case report, differential diagnosis and literature review]F Haverkamp, K Zerres, H Fahnenstich, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Klinische Padiatrie|May 1, 1996
[X-chromosomal recessive hydrocephalus internus: a separate disease picture? 2 further case reports and review of the literature]F Haverkamp, A Krämer, H Fahnenstich, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|July 30, 2013
Initial knowledge at radiation protection courses from 2005-2013 (3): tendencies and conclusionsU F Haverkamp, B A Pruemer, A Fahrmer
European Journal of Pediatrics|December 3, 1998
False-positive serological tests for Lyme disease in facial palsy and varicella zoster meningo-encephalitisJ Woelfle, B Wilske, F Haverkamp, et al.
Klinische Padiatrie|January 31, 1998
[Mitochondrial diseases]J D Nagel, F Haverkamp, M J Lentze
European Journal of Ophthalmology|October 28, 2004
Intraocular pressure, safety and quality of life in glaucoma patients switching to latanoprost from adjunctive and monotherapy treatmentsF Haverkamp, S Wuensch, M Fuchs, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 25, 2000
Symptomatic versus substitution growth hormone therapy in short children: from auxology towards a comprehensive multidimensional assessment of short stature and related interventionsF Haverkamp, U Eiholzer, M B Ranke, et al.
Klinische Padiatrie|October 26, 2000
[Processes of body perception and their therapeutic use in pediatrics. From nonspecific relaxation therapy to training to recognize disease-specific symptoms]M Noeker, U von Rüden, D Staab, et al.
Klinische Padiatrie|January 30, 2004
[Methodological perspectives for the assessment of adaptation in chronic diseases, exemplified by asthma bronchiale in childhood]F Haverkamp, D Staab, K Müller-Sinik, et al.
Clinical Genetics|June 2, 2007
Isolated cystinuria (OMIM 238200) is not a separate entity but is caused by a mutation in the cystinuria gene SLC7A9T Eggermann, M Elbracht, F Haverkamp, et al.
Klinische Padiatrie|November 1, 1990
[7-week-old infant with a hydrolethalus syndrome: case report, differential diagnosis and literature review]F Haverkamp, K Zerres, H Fahnenstich, et al.
Pageof 7