Search Results - "MacLaughlin, Eithne"

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    Clinical Findings and Lung Pathology in Children with Cystic Fibrosis by Hamutcu, Refika, Rowland, Jon M, Horn, Monica V, Kaminsky, Cornelia, MacLaughlin, Eithne F, Starnes, Vaughn A, Woo, Marlyn S

    “…Cystic fibrosis pulmonary disease is assessed by pulmonary function tests, arterial blood gases, and chest X-rays, but the correlation with lung pathology is…”
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    Prognosis in pediatric idiopathic pulmonary hemosiderosis by Saeed, M M, Woo, M S, MacLaughlin, E F, Margetis, M F, Keens, T G

    Published in Chest (01-09-1999)
    “…Previously, IPH patients have been reported to have an average survival of 2.5 years. However, at our institution, many IPH patients have survived longer than…”
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    Comparison of outcomes between living donor and cadaveric lung transplantation in children by Starnes, Vaughn A, Woo, Marlyn S, MacLaughlin, Eithne F, Horn, Monica V, Wong, Pierre C, Rowland, Jon M, Durst, Carolyn L, Wells, Winfield J, Barr, Mark L

    Published in The Annals of thoracic surgery (01-12-1999)
    “…Background. Long-term survival in lung transplant is limited by bronchiolitis obliterans (BOS). We compared outcomes in pediatric living donor bilateral lobar…”
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    Bordetella bronchiseptica infection in pediatric lung transplant recipients by Ner, Zarah, A. Ross, Lawrence, Horn, Monica V., Keens, Thomas G., MacLaughlin, Eithne F., Starnes, Vaughn A., Woo, Marlyn S.

    Published in Pediatric transplantation (01-10-2003)
    “…: Bordetella bronchiseptica are small, pleomorphic Gram‐negative coccobacilli which are commensal organisms in the upper respiratory tract of many wild and…”
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    Does lung growth occur when mature lobes are transplanted into children? by Sritippayawan, Suchada, Keens, Thomas G., Horn, Monica V., MacLaughlin, Eithne F., Barr, Mark L., Starnes, Vaughn A., Woo, Marlyn S.

    Published in Pediatric transplantation (01-12-2002)
    “…: Lung volume increases after living donor lobar lung transplantation (LD) in children. The mechanism responsible for this increase may be alveolarization…”
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    Acute neurological deficits in a young adult with cystic fibrosis by Sritippayawan, Suchada, MacLaughlin, Eithne F., Woo, Marlyn S.

    Published in Pediatric pulmonology (01-02-2003)
    “…An abrupt onset of a neurological deficit is a rare occurrence in patients with cystic fibrosis (CF). As many CF patients have indwelling intravenous…”
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    Bronchiolitis obliterans is not the primary cause of death in pediatric living donor lobar lung transplant recipients by Woo, M S, MacLaughlin, E F, Horn, M V, Szmuszkovicz, J R, Barr, M L, Starnes, V A

    “…Obliterative bronchiolitis (OB) is the chief cause of mortality in cadaveric lung transplant patients (CL). But, is OB the primary cause of mortality for…”
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    Psychosocial responses of adolescent cystic fibrosis patients to lung transplantation by Durst, Carolyn L., Horn, Monica V., MacLaughlin, Eithne F., Bowman, C. Michael, Starnes, Vaughn A., Woo, Marlyn S.

    Published in Pediatric transplantation (01-02-2001)
    “…: What psychosocial issues do adolescent cystic fibrosis (CF) patients experience after undergoing lung transplantation (Tx)? The aim of this study was to…”
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    Cor triatriatum: A cause of hemoptysis by Sritippayawan, Suchada, Margetis, Monique F., MacLaughlin, Eithne F., Achermann, Ruben, Wells, Winfield J., Davidson Ward, Sally L.

    Published in Pediatric pulmonology (01-11-2002)
    “…Hemoptysis can be caused by either pulmonary or extrapulmonary causes. Congenital heart disease should be considered as a possible cause in patients who have…”
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    Paecilomyces variotii in a pediatric patient with lung transplantation by Das, Aninda, MacLaughlin, Eithne F., Ross, Lawrence A., Monforte, Hector L., Horn, Monica V., Lam, Gennie L. J., Mason, Wilbert H.

    Published in Pediatric transplantation (01-11-2000)
    “…: Aspergillus has been noted to be the most common species of filamentous fungus isolated from the airways of lung transplantation (Tx) patients. In general,…”
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    Systemic pseudohypoaldosteronism from deletion of the promoter region of the human Beta epithelial na(+) channel subunit by Thomas, Christie P, Zhou, Jackie, Liu, Kang Z, Mick, Verity E, MacLaughlin, Eithne, Knowles, Michael

    “…Systemic pseudohypoaldosteronism type I (PHAI) is an autosomal recessive disorder that arises from loss of function mutations of the alpha, beta, or gamma…”
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    Sickle cell chronic lung disease: prior morbidity and the risk of pulmonary failure by Powars, D, Weidman, J A, Odom-Maryon, T, Niland, J C, Johnson, C

    Published in Medicine (Baltimore) (01-01-1988)
    “…Sickle cell chronic lung disease (SCLD) is a prime contributor to mortality in young adult patients with sickle cell disease, especially those with sickle cell…”
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    Living donor lobar lung transplantation: the pediatric experience by Woo, M S, MacLaughlin, E F, Horn, M V, Wong, P C, Rowland, J M, Barr, M L, Starnes, V A

    Published in Pediatric transplantation (01-08-1998)
    “…Living donor (LD) lobar lung transplantation is now an accepted alternative to cadaveric lung transplantation in selected patients with end-stage lung disease…”
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    Long-term ventilatory support in spinal muscular atrophy by Gilgoff, I S, Kahlstrom, E, MacLaughlin, E, Keens, T G

    Published in The Journal of pediatrics (01-12-1989)
    “…Before ethical issues regarding prolonging life in patients with degenerative disease can be considered, the quality of life with medical intervention must be…”
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    Tracheotomy in infants and young children: the changing perspective 1970-1985 by Line, Jr, W S, Hawkins, D B, Kahlstrom, E J, MacLaughlin, E F, Ensley, J L

    Published in The Laryngoscope (01-05-1986)
    “…One hundred fifty-three children 3 years of age or younger who had tracheotomies performed during the past 15 years are reviewed. During this time, short-term…”
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    Mycobacterial cervical adenitis in children: medical and surgical management by Hawkins, D B, Shindo, M L, Kahlstrom, E J, MacLaughlin, E F

    Published in Ear, nose, & throat journal (01-11-1993)
    “…This is a review of the treatment results of cervicofacial mycobacterial adenitis in 85 children and adolescents. Twenty-three patients were treated with only…”
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