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L C Wilson

Showing results (21-30 of 36) with videos related to

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Postgraduate Medical Journal|September 1, 1973
A double-blind clinical trial of griseofulvin in patients with Raynaud's phenomenonS Sabri, R F Higgins, V C Roberts, et al.
Journal of Medical Genetics|June 7, 2005
Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotypeS Shackleton, D T Smallwood, P Clayton, et al.
The British Journal of Dermatology|April 27, 2007
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literatureJ Mazereeuw-Hautier, L C Wilson, S Mohammed, et al.
The Journal of Physiology|November 13, 2020
Indomethacin markedly blunts cerebral perfusion and reactivity, with little cognitive consequence in healthy young and older adultsL N Shoemaker, L C Wilson, S J E Lucas, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|June 9, 2004
Familial syndromic duodenal atresia: Feingold syndromeM Holder-Espinasse, Z Ahmad, J Hamill, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|December 8, 2017
Independent and interactive effects of incremental heat strain, orthostatic stress, and mild hypohydration on cerebral perfusionR A I Lucas, L C Wilson, P N Ainslie, et al.
American Journal of Clinical Oncology|October 1, 1984
Five-year cure of cervical cancer treated using californium-252 neutron brachytherapyY Maruyama, J R van Nagell, J Yoneda, et al.
Human Molecular Genetics|October 1, 1995
A deletion hot-spot in exon 7 of the Gs alpha gene (GNAS1) in patients with Albright hereditary osteodystrophyS Yu, D Yu, B E Hainline, et al.
American Journal of Human Genetics|February 1, 1995
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.
International Journal of Radiation Oncology, Biology, Physics|December 1, 1980
A clinical trial for advanced cervico-vaginal pelvic carcinomas using Californium Cf-252 fast neutron therapy: report of early responsesY Maruyama, J Yoneda, H Krolikiewicz, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Postgraduate Medical Journal|September 1, 1973
A double-blind clinical trial of griseofulvin in patients with Raynaud's phenomenonS Sabri, R F Higgins, V C Roberts, et al.
Journal of Medical Genetics|June 7, 2005
Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotypeS Shackleton, D T Smallwood, P Clayton, et al.
The British Journal of Dermatology|April 27, 2007
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literatureJ Mazereeuw-Hautier, L C Wilson, S Mohammed, et al.
The Journal of Physiology|November 13, 2020
Indomethacin markedly blunts cerebral perfusion and reactivity, with little cognitive consequence in healthy young and older adultsL N Shoemaker, L C Wilson, S J E Lucas, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|June 9, 2004
Familial syndromic duodenal atresia: Feingold syndromeM Holder-Espinasse, Z Ahmad, J Hamill, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|December 8, 2017
Independent and interactive effects of incremental heat strain, orthostatic stress, and mild hypohydration on cerebral perfusionR A I Lucas, L C Wilson, P N Ainslie, et al.
American Journal of Clinical Oncology|October 1, 1984
Five-year cure of cervical cancer treated using californium-252 neutron brachytherapyY Maruyama, J R van Nagell, J Yoneda, et al.
Human Molecular Genetics|October 1, 1995
A deletion hot-spot in exon 7 of the Gs alpha gene (GNAS1) in patients with Albright hereditary osteodystrophyS Yu, D Yu, B E Hainline, et al.
American Journal of Human Genetics|February 1, 1995
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.
International Journal of Radiation Oncology, Biology, Physics|December 1, 1980
A clinical trial for advanced cervico-vaginal pelvic carcinomas using Californium Cf-252 fast neutron therapy: report of early responsesY Maruyama, J Yoneda, H Krolikiewicz, et al.
Pageof 4