M Daras|A J Spiro - JoVE Visualize

Showing results (41-50 of 47) with videos related to

Pageof 5

Sort By:

You have reached the last page of results.This site can display upto 47 results.

American Journal of Human Genetics|November 1, 1988

Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.

Iscience|January 13, 2025

An eco-evolutionary perspective on antimicrobial resistance in the context of One HealthMisshelle Bustamante, Siyu Mei, Ines M Daras, et al.

Pediatric Neurology|November 1, 1993

Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophyD A Paul, L S Goldsmith, D K Miles, et al.

Annals of Neurology|November 1, 1985

Neurological complications in infants and children with acquired immune deficiency syndromeA L Belman, M H Ultmann, D Horoupian, et al.

The Journal of Pediatrics|January 1, 1986

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activitiesS Goldfischer, J Collins, I Rapin, et al.

Science (New York, N.Y.)|October 5, 1973

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndromeS Goldfischer, C L Moore, A B Johnson, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 12, 2001

Lack of correlation of functional scintigraphy with (99m)technetium-methoxyisobutylisonitrile with histological necrosis following induction chemotherapy or measures of P-glycoprotein expression in high-grade osteosarcomaR Gorlick, A C Liao, C Antonescu, et al.

Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 47 results.

American Journal of Human Genetics|November 1, 1988

Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.

Iscience|January 13, 2025

An eco-evolutionary perspective on antimicrobial resistance in the context of One HealthMisshelle Bustamante, Siyu Mei, Ines M Daras, et al.

Pediatric Neurology|November 1, 1993

Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophyD A Paul, L S Goldsmith, D K Miles, et al.

Annals of Neurology|November 1, 1985

Neurological complications in infants and children with acquired immune deficiency syndromeA L Belman, M H Ultmann, D Horoupian, et al.

The Journal of Pediatrics|January 1, 1986

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activitiesS Goldfischer, J Collins, I Rapin, et al.

Science (New York, N.Y.)|October 5, 1973

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndromeS Goldfischer, C L Moore, A B Johnson, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 12, 2001

Lack of correlation of functional scintigraphy with (99m)technetium-methoxyisobutylisonitrile with histological necrosis following induction chemotherapy or measures of P-glycoprotein expression in high-grade osteosarcomaR Gorlick, A C Liao, C Antonescu, et al.

Pageof 5