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Showing results (101-110 of 109) with videos related to

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Nature Genetics|June 30, 2001
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humansS M Sisodiya, S L Free, K A Williamson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2006
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypesFaisal Idrees, Agnes Bloch-Zupan, Samantha L Free, et al.
Epilepsia|March 15, 2006
Role of SOX2 mutations in human hippocampal malformations and epilepsySanjay M Sisodiya, Nicola K Ragge, Gianpiero L Cavalleri, et al.
European Journal of Clinical Pharmacology|April 24, 2026
Effects of renal impairment on the pharmacokinetics, safety, and tolerability of pudexacianinium (ASP5354) after IV administration: a mechanistic explorationTomoki Kojima, Masako Saito, Toshihiro Matsuda, et al.
Clinical and Translational Science|July 21, 2017
Leveraging a Clinical Phase Ib Proof-of-Concept Study for the GPR40 Agonist MK-8666 in Patients With Type 2 Diabetes for Model-Informed Phase II Dose SelectionA W Krug, P Vaddady, R A Railkar, et al.
Neurology|January 5, 2002
Quantitative hippocampal MRI and intractable temporal lobe epilepsy. 1995W Van Paesschen, S Sisodiya, A Connelly, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
Clinical Pharmacology and Therapeutics|January 27, 2012
A randomized, placebo-controlled study of the effects of telcagepant on exercise time in patients with stable anginaB R Chaitman, A P Ho, M O Behm, et al.
Journal of Medical Genetics|January 24, 2007
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutationSanjay M Sisodiya, Pamela J Thompson, Anna Need, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
Nature Genetics|June 30, 2001
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humansS M Sisodiya, S L Free, K A Williamson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2006
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypesFaisal Idrees, Agnes Bloch-Zupan, Samantha L Free, et al.
Epilepsia|March 15, 2006
Role of SOX2 mutations in human hippocampal malformations and epilepsySanjay M Sisodiya, Nicola K Ragge, Gianpiero L Cavalleri, et al.
European Journal of Clinical Pharmacology|April 24, 2026
Effects of renal impairment on the pharmacokinetics, safety, and tolerability of pudexacianinium (ASP5354) after IV administration: a mechanistic explorationTomoki Kojima, Masako Saito, Toshihiro Matsuda, et al.
Clinical and Translational Science|July 21, 2017
Leveraging a Clinical Phase Ib Proof-of-Concept Study for the GPR40 Agonist MK-8666 in Patients With Type 2 Diabetes for Model-Informed Phase II Dose SelectionA W Krug, P Vaddady, R A Railkar, et al.
Neurology|January 5, 2002
Quantitative hippocampal MRI and intractable temporal lobe epilepsy. 1995W Van Paesschen, S Sisodiya, A Connelly, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
Clinical Pharmacology and Therapeutics|January 27, 2012
A randomized, placebo-controlled study of the effects of telcagepant on exercise time in patients with stable anginaB R Chaitman, A P Ho, M O Behm, et al.
Journal of Medical Genetics|January 24, 2007
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutationSanjay M Sisodiya, Pamela J Thompson, Anna Need, et al.
Pageof 11