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M Philippart

Showing results (71-80 of 85) with videos related to

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Harmful Algae|August 9, 2022
Mixotrophy in the bloom-forming genus Phaeocystis and other haptophytesSebastiaan Koppelle, David López-Escardó, Corina P D Brussaard, et al.
American Journal of Ophthalmology|September 15, 1984
Congenital corneal opacification secondary to Bowman's layer dysgenesisD J Apple, R J Olson, G R Jones, et al.
Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
Journal of the Neurological Sciences|May 1, 1974
The Schwartz-Jampel syndrome. Its clinical, physiological and histological expressionsW M Fowler, R B Layzer, R G Taylor, et al.
Parasitology|November 30, 2017
Trophic relationship between the invasive parasitic copepod Mytilicola orientalis and its native blue mussel (Mytilus edulis) hostM Anouk Goedknegt, David Shoesmith, A Sarina Jung, et al.
Annals of Neurology|April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypesB A Minassian, T M DeLorey, R W Olsen, et al.
Alimentary Pharmacology & Therapeutics|August 29, 2013
Systematic review: probiotics in the management of lower gastrointestinal symptoms in clinical practice -- an evidence-based international guideA P S Hungin, C Mulligan, B Pot, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Neurology|April 14, 2004
Leukoencephalopathy, cerebral calcifications, and cysts: new observationsL M Nagae-Poetscher, G Bibat, M Philippart, et al.
Neurology|June 13, 2001
MeCP2 mutations in children with and without the phenotype of Rett syndromeK Hoffbuhr, J M Devaney, B LaFleur, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Harmful Algae|August 9, 2022
Mixotrophy in the bloom-forming genus Phaeocystis and other haptophytesSebastiaan Koppelle, David López-Escardó, Corina P D Brussaard, et al.
American Journal of Ophthalmology|September 15, 1984
Congenital corneal opacification secondary to Bowman's layer dysgenesisD J Apple, R J Olson, G R Jones, et al.
Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
Journal of the Neurological Sciences|May 1, 1974
The Schwartz-Jampel syndrome. Its clinical, physiological and histological expressionsW M Fowler, R B Layzer, R G Taylor, et al.
Parasitology|November 30, 2017
Trophic relationship between the invasive parasitic copepod Mytilicola orientalis and its native blue mussel (Mytilus edulis) hostM Anouk Goedknegt, David Shoesmith, A Sarina Jung, et al.
Annals of Neurology|April 18, 1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypesB A Minassian, T M DeLorey, R W Olsen, et al.
Alimentary Pharmacology & Therapeutics|August 29, 2013
Systematic review: probiotics in the management of lower gastrointestinal symptoms in clinical practice -- an evidence-based international guideA P S Hungin, C Mulligan, B Pot, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Neurology|April 14, 2004
Leukoencephalopathy, cerebral calcifications, and cysts: new observationsL M Nagae-Poetscher, G Bibat, M Philippart, et al.
Neurology|June 13, 2001
MeCP2 mutations in children with and without the phenotype of Rett syndromeK Hoffbuhr, J M Devaney, B LaFleur, et al.
Pageof 9