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Should all infants with delayed umbilical cord separation be investigated for leucocyte adhesion deficiency?

Should all infants with delayed umbilical cord separation be investigated for leucocyte adhesion... Archimedes 2 Keskinen H, Lukkarinen H, Korhonen K, et al. The lifetime risk of pneumonia in patients screening test requires a clinically important disease. LAD is a with neuromuscular scoliosis at a mean age of 21 years: the role of spinal deformity rare (1:100 000), hereditary, autosomal recessive primary immu- surgery. J Child Orthop 2015;9:357–64. nodeficiency, with three subtypes. LAD causes defects in the 3 Inal- Ince D, Savci S, Arikan H, et al. Effects of scoliosis on respiratory muscle strength in leucocyte adhesion cascade (a four- step process involving patients with neuromuscular disorders. Spine J 2009;9:981–6. rolling, firm arrest, postarrest modifications and transmigration 4 Alexander WM, Smith M, Freeman BJC, et al. The effect of posterior spinal fusion on respiratory function in Duchenne muscular dystrophy. Eur Spine J 2013;22:411–6. into tissues ) preventing neutrophil migration to the site of tissue 5 Velasco MV, Colin AA, Zurakowski D, et al. Posterior spinal fusion for scoliosis in infection (online supplemental figure 1). duchenne muscular dystrophy diminishes the rate of respiratory decline. Spine LAD-I and LAD -III are fatal in infancy/childhood without 2007;32:459–65. haematopoietic stem cell transplantation. 6 Suk KS, Lee BH, Lee HM, et al. Functional outcomes in Duchenne muscular dystrophy Establishing a case for http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Disease in Childhood British Medical Journal

Should all infants with delayed umbilical cord separation be investigated for leucocyte adhesion deficiency?

Should all infants with delayed umbilical cord separation be investigated for leucocyte adhesion deficiency?

Archives of Disease in Childhood , Volume 106 (12) – Dec 1, 2021

Abstract

Archimedes 2 Keskinen H, Lukkarinen H, Korhonen K, et al. The lifetime risk of pneumonia in patients screening test requires a clinically important disease. LAD is a with neuromuscular scoliosis at a mean age of 21 years: the role of spinal deformity rare (1:100 000), hereditary, autosomal recessive primary immu- surgery. J Child Orthop 2015;9:357–64. nodeficiency, with three subtypes. LAD causes defects in the 3 Inal- Ince D, Savci S, Arikan H, et al. Effects of scoliosis on respiratory muscle strength in leucocyte adhesion cascade (a four- step process involving patients with neuromuscular disorders. Spine J 2009;9:981–6. rolling, firm arrest, postarrest modifications and transmigration 4 Alexander WM, Smith M, Freeman BJC, et al. The effect of posterior spinal fusion on respiratory function in Duchenne muscular dystrophy. Eur Spine J 2013;22:411–6. into tissues ) preventing neutrophil migration to the site of tissue 5 Velasco MV, Colin AA, Zurakowski D, et al. Posterior spinal fusion for scoliosis in infection (online supplemental figure 1). duchenne muscular dystrophy diminishes the rate of respiratory decline. Spine LAD-I and LAD -III are fatal in infancy/childhood without 2007;32:459–65. haematopoietic stem cell transplantation. 6 Suk KS, Lee BH, Lee HM, et al. Functional outcomes in Duchenne muscular dystrophy Establishing a case for

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References (27)

Publisher
British Medical Journal
Copyright
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
ISSN
0003-9888
eISSN
1468-2044
DOI
10.1136/archdischild-2020-321313
Publisher site
See Article on Publisher Site

Abstract

Archimedes 2 Keskinen H, Lukkarinen H, Korhonen K, et al. The lifetime risk of pneumonia in patients screening test requires a clinically important disease. LAD is a with neuromuscular scoliosis at a mean age of 21 years: the role of spinal deformity rare (1:100 000), hereditary, autosomal recessive primary immu- surgery. J Child Orthop 2015;9:357–64. nodeficiency, with three subtypes. LAD causes defects in the 3 Inal- Ince D, Savci S, Arikan H, et al. Effects of scoliosis on respiratory muscle strength in leucocyte adhesion cascade (a four- step process involving patients with neuromuscular disorders. Spine J 2009;9:981–6. rolling, firm arrest, postarrest modifications and transmigration 4 Alexander WM, Smith M, Freeman BJC, et al. The effect of posterior spinal fusion on respiratory function in Duchenne muscular dystrophy. Eur Spine J 2013;22:411–6. into tissues ) preventing neutrophil migration to the site of tissue 5 Velasco MV, Colin AA, Zurakowski D, et al. Posterior spinal fusion for scoliosis in infection (online supplemental figure 1). duchenne muscular dystrophy diminishes the rate of respiratory decline. Spine LAD-I and LAD -III are fatal in infancy/childhood without 2007;32:459–65. haematopoietic stem cell transplantation. 6 Suk KS, Lee BH, Lee HM, et al. Functional outcomes in Duchenne muscular dystrophy Establishing a case for

Journal

Archives of Disease in ChildhoodBritish Medical Journal

Published: Dec 1, 2021

Keywords: cell biologymolecular biologygeneticsepidemiology

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