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F S Cole

Showing results (51-60 of 63) with videos related to

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Transactions of the Association of American Physicians|January 1, 1985
A selective defect in secretion of alpha 1-proteinase inhibitor PiZZ demonstrated in surrogate and primary extrahepatic cell cultureD H Perlmutter, R M Kay, F S Cole, et al.
The New England Journal of Medicine|July 4, 1985
The molecular basis for genetic deficiency of the second component of human complementF S Cole, A S Whitehead, H S Auerbach, et al.
The Journal of Pediatrics|September 1, 1994
Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacementA Hamvas, F S Cole, D E deMello, et al.
Pediatric Nephrology (Berlin, Germany)|June 13, 2022
Lethal neonatal respiratory failure due to biallelic variants in BBS1 and monoallelic variant in TTC21BLuke Viehl, Daniel J Wegner, Stanley P Hmiel, et al.
Pediatrics|March 4, 2000
Population-based estimates of surfactant protein B deficiencyF S Cole, A Hamvas, P Rubinstein, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|April 1, 1995
School-based AIDS education for adolescentsJ Sunwood, A Brenman, J Escobedo, et al.
Pediatrics|March 1, 1997
Risk status at discharge and cause of death for postneonatal infant deaths: a total population studyA Kempe, P H Wise, N S Wampler, et al.
The New England Journal of Medicine|June 20, 1996
The influence of the wider use of surfactant therapy on neonatal mortality among blacks and whitesA Hamvas, P H Wise, R K Yang, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal locationB Royer-Pokora, L M Kunkel, A P Monaco, et al.
Nature|July 3, 1986
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal locationB Royer-Pokora, L M Kunkel, A P Monaco, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Transactions of the Association of American Physicians|January 1, 1985
A selective defect in secretion of alpha 1-proteinase inhibitor PiZZ demonstrated in surrogate and primary extrahepatic cell cultureD H Perlmutter, R M Kay, F S Cole, et al.
The New England Journal of Medicine|July 4, 1985
The molecular basis for genetic deficiency of the second component of human complementF S Cole, A S Whitehead, H S Auerbach, et al.
The Journal of Pediatrics|September 1, 1994
Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacementA Hamvas, F S Cole, D E deMello, et al.
Pediatric Nephrology (Berlin, Germany)|June 13, 2022
Lethal neonatal respiratory failure due to biallelic variants in BBS1 and monoallelic variant in TTC21BLuke Viehl, Daniel J Wegner, Stanley P Hmiel, et al.
Pediatrics|March 4, 2000
Population-based estimates of surfactant protein B deficiencyF S Cole, A Hamvas, P Rubinstein, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|April 1, 1995
School-based AIDS education for adolescentsJ Sunwood, A Brenman, J Escobedo, et al.
Pediatrics|March 1, 1997
Risk status at discharge and cause of death for postneonatal infant deaths: a total population studyA Kempe, P H Wise, N S Wampler, et al.
The New England Journal of Medicine|June 20, 1996
The influence of the wider use of surfactant therapy on neonatal mortality among blacks and whitesA Hamvas, P H Wise, R K Yang, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal locationB Royer-Pokora, L M Kunkel, A P Monaco, et al.
Nature|July 3, 1986
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal locationB Royer-Pokora, L M Kunkel, A P Monaco, et al.
Pageof 7