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M Pfister

Showing results (181-190 of 752) with videos related to

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 11, 2012
[Cytokine determination from vitreous samples in retinal vascular diseases]M Pfister, F H Koch, J Cinatl, et al.
Children (Basel, Switzerland)|June 28, 2023
Reduced Hippocampal Volumes in Children with History of Hypoxic Ischemic Encephalopathy after Therapeutic HypothermiaKatie M Pfister, Sally M Stoyell, Zachary R Miller, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Diseases of the Colon and Rectum|September 28, 1998
Excision of trocar sites reduces tumor implantation in an animal modelJ S Wu, L W Guo, M B Ruiz, et al.
American Journal of Ophthalmology|March 10, 2015
Intraocular Medulloepitheliomas and Embryonal Tumors With Multilayered Rosettes of the Brain: Comparative Roles of LIN28A and C19MCFrederick A Jakobiec, Marcel Kool, Anna M Stagner, et al.
Cancers|July 18, 2020
Rapid and Sensitive Quantification of Osimertinib in Human Plasma Using a Fully Validated MALDI-IM-MS/MS AssayMargaux Fresnais, André Roth, Kathrin I Foerster, et al.
Molecular Genetics and Metabolism|September 20, 2000
A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemiaA Chango, N Emery-Fillon, G P de Courcy, et al.
Pageof 76

Showing results (181-190 of 752) with videos related to

Sort By:
Pageof 76
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 11, 2012
[Cytokine determination from vitreous samples in retinal vascular diseases]M Pfister, F H Koch, J Cinatl, et al.
Children (Basel, Switzerland)|June 28, 2023
Reduced Hippocampal Volumes in Children with History of Hypoxic Ischemic Encephalopathy after Therapeutic HypothermiaKatie M Pfister, Sally M Stoyell, Zachary R Miller, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Diseases of the Colon and Rectum|September 28, 1998
Excision of trocar sites reduces tumor implantation in an animal modelJ S Wu, L W Guo, M B Ruiz, et al.
American Journal of Ophthalmology|March 10, 2015
Intraocular Medulloepitheliomas and Embryonal Tumors With Multilayered Rosettes of the Brain: Comparative Roles of LIN28A and C19MCFrederick A Jakobiec, Marcel Kool, Anna M Stagner, et al.
Cancers|July 18, 2020
Rapid and Sensitive Quantification of Osimertinib in Human Plasma Using a Fully Validated MALDI-IM-MS/MS AssayMargaux Fresnais, André Roth, Kathrin I Foerster, et al.
Molecular Genetics and Metabolism|September 20, 2000
A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemiaA Chango, N Emery-Fillon, G P de Courcy, et al.
Pageof 76