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Evaluation and treatment of syncope in infants.

Progress in pediatric cardiology

Kochilas L, Tanel RE.
PMID: 11457676
Prog Pediatr Cardiol. 2001 Aug;13(2):71-82. doi: 10.1016/s1058-9813(01)00090-x.

Syncope in the infant and newborn occurs as a loss of consciousness due to a variety of etiologies. Because syncope at this age may be a harbinger of sudden infant death, the symptom provokes anxiety and challenges clinicians to...

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Kochilas L, Tanel RE. Evaluation and treatment of syncope in infants. Prog Pediatr Cardiol. 2001;13(2):71-82doi: 10.1016/s1058-9813(01)00090-x.
Kochilas, L., & Tanel, R. E. (2001). Evaluation and treatment of syncope in infants. Progress in pediatric cardiology, 13(2), 71-82. https://doi.org/10.1016/s1058-9813(01)00090-x
Kochilas, L, and Tanel, R E.. "Evaluation and treatment of syncope in infants." Progress in pediatric cardiology vol. 13,2 (2001): 71-82. doi: https://doi.org/10.1016/s1058-9813(01)00090-x
Kochilas L, Tanel RE. Evaluation and treatment of syncope in infants. Prog Pediatr Cardiol. 2001 Aug;13(2):71-82. doi: 10.1016/s1058-9813(01)00090-x. PMID: 11457676.
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Fog2 is required for normal diaphragm and lung development in mice and humans.

PLoS genetics

Ackerman KG, Herron BJ, Vargas SO, Huang H, Tevosian SG, Kochilas L, Rao C, Pober BR, Babiuk RP, Epstein JA, Greer JJ, Beier DR.
PMID: 16103912
PLoS Genet. 2005 Jul;1(1):58-65. doi: 10.1371/journal.pgen.0010010. Epub 2005 Jun 17.

Congenital diaphragmatic hernia and other congenital diaphragmatic defects are associated with significant mortality and morbidity in neonates; however, the molecular basis of these developmental anomalies is unknown. In an analysis of E18.5 embryos derived from mice treated with N-ethyl-N-nitrosourea,...

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Ackerman KG, Herron BJ, Vargas SO, et al. Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet. 2005;1(1):58-65doi: 10.1371/journal.pgen.0010010.
Ackerman, K. G., Herron, B. J., Vargas, S. O., Huang, H., Tevosian, S. G., Kochilas, L., Rao, C., Pober, B. R., Babiuk, R. P., Epstein, J. A., Greer, J. J., & Beier, D. R. (2005). Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS genetics, 1(1), 58-65. https://doi.org/10.1371/journal.pgen.0010010
Ackerman, Kate G, et al. "Fog2 is required for normal diaphragm and lung development in mice and humans." PLoS genetics vol. 1,1 (2005): 58-65. doi: https://doi.org/10.1371/journal.pgen.0010010
Ackerman KG, Herron BJ, Vargas SO, Huang H, Tevosian SG, Kochilas L, Rao C, Pober BR, Babiuk RP, Epstein JA, Greer JJ, Beier DR. Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet. 2005 Jul;1(1):58-65. doi: 10.1371/journal.pgen.0010010. Epub 2005 Jun 17. PMID: 16103912; PMCID: PMC1183529.
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Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns.

Medical devices (Auckland, N.Z.)

Engel MS, Kochilas LK.
PMID: 27468253
Med Devices (Auckl). 2016 Jul 11;9:199-203. doi: 10.2147/MDER.S102146. eCollection 2016.

Congenital heart disease (CHD) is one of the most common birth defects, with an incidence of nine out of every 1,000 live births. The mortality of infants with CHD has decreased over the past 3 decades, but significant morbidity...

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Engel MS, Kochilas LK. Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns. Med Devices (Auckl). 2016;9:199-203doi: 10.2147/MDER.S102146.
Engel, M. S., & Kochilas, L. K. (2016). Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns. Medical devices (Auckland, N.Z.), 9199-203. https://doi.org/10.2147/MDER.S102146
Engel, Melissa S, and Kochilas, Lazaros K. "Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns." Medical devices (Auckland, N.Z.) vol. 9 (2016): 199-203. doi: https://doi.org/10.2147/MDER.S102146
Engel MS, Kochilas LK. Pulse oximetry screening: a review of diagnosing critical congenital heart disease in newborns. Med Devices (Auckl). 2016 Jul 11;9:199-203. doi: 10.2147/MDER.S102146. eCollection 2016. PMID: 27468253; PMCID: PMC4946827.
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Reply.

The Journal of pediatrics

Knutson S, Kochilas L.
PMID: 27989410
J Pediatr. 2017 Apr;183:201. doi: 10.1016/j.jpeds.2016.11.061. Epub 2016 Dec 15.

No abstract available.

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Knutson S, Kochilas L. Reply. J Pediatr. 2016;183:201doi: 10.1016/j.jpeds.2016.11.061.
Knutson, S., & Kochilas, L. (2017). Reply. The Journal of pediatrics, 183201. https://doi.org/10.1016/j.jpeds.2016.11.061
Knutson, Stacie, and Kochilas, Lazaros. "Reply." The Journal of pediatrics vol. 183 (2017): 201. doi: https://doi.org/10.1016/j.jpeds.2016.11.061
Knutson S, Kochilas L. Reply. J Pediatr. 2017 Apr;183:201. doi: 10.1016/j.jpeds.2016.11.061. Epub 2016 Dec 15. PMID: 27989410.
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Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome.

The Journal of pediatrics

Alam S, Claxton JS, Mortillo M, Sassis L, Kefala-Karli P, Silberbach M, Kochilas L, Wechsler SB.
PMID: 34450123
J Pediatr. 2021 Dec;239:187-192.e1. doi: 10.1016/j.jpeds.2021.08.034. Epub 2021 Aug 24.

OBJECTIVE: To evaluate long-term survival in patients with Turner syndrome after congenital heart surgery with a focus on left heart obstructive lesions (LHOLs).STUDY DESIGN: We queried the Pediatric Cardiac Care Consortium, a US-based registry of congenital heart surgery, for...

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Alam S, Claxton JS, Mortillo M, et al. Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. J Pediatr. 2021;239:187-192.e1doi: 10.1016/j.jpeds.2021.08.034.
Alam, S., Claxton, J. S., Mortillo, M., Sassis, L., Kefala-Karli, P., Silberbach, M., Kochilas, L., & Wechsler, S. B. (2021). Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. The Journal of pediatrics, 239187-192.e1. https://doi.org/10.1016/j.jpeds.2021.08.034
Alam, Sabikha, et al. "Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome." The Journal of pediatrics vol. 239 (2021): 187-192.e1. doi: https://doi.org/10.1016/j.jpeds.2021.08.034
Alam S, Claxton JS, Mortillo M, Sassis L, Kefala-Karli P, Silberbach M, Kochilas L, Wechsler SB. Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. J Pediatr. 2021 Dec;239:187-192.e1. doi: 10.1016/j.jpeds.2021.08.034. Epub 2021 Aug 24. PMID: 34450123; PMCID: PMC8626205.
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Association of Digoxin With Preserved Echocardiographic Indices in the Interstage Period: A Possible Mechanism to Explain Improved Survival?.

Journal of the American Heart Association

Batsis M, Kochilas L, Chin AJ, Kelleman M, Ferguson E, Oster ME.
PMID: 34854311
J Am Heart Assoc. 2021 Dec 07;10(23):e021443. doi: 10.1161/JAHA.121.021443. Epub 2021 Dec 02.

Background For patients with hypoplastic left heart syndrome, digoxin has been associated with reduced interstage mortality after the Norwood operation, but the mechanism of this benefit remains unclear. Preservation of right ventricular (RV) echocardiographic indices has been associated with...

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Batsis M, Kochilas L, Chin AJ, et al. Association of Digoxin With Preserved Echocardiographic Indices in the Interstage Period: A Possible Mechanism to Explain Improved Survival?. J Am Heart Assoc. 2021;10(23):e021443doi: 10.1161/JAHA.121.021443.
Batsis, M., Kochilas, L., Chin, A. J., Kelleman, M., Ferguson, E., & Oster, M. E. (2021). Association of Digoxin With Preserved Echocardiographic Indices in the Interstage Period: A Possible Mechanism to Explain Improved Survival?. Journal of the American Heart Association, 10(23), e021443. https://doi.org/10.1161/JAHA.121.021443
Batsis, Maria, et al. "Association of Digoxin With Preserved Echocardiographic Indices in the Interstage Period: A Possible Mechanism to Explain Improved Survival?." Journal of the American Heart Association vol. 10,23 (2021): e021443. doi: https://doi.org/10.1161/JAHA.121.021443
Batsis M, Kochilas L, Chin AJ, Kelleman M, Ferguson E, Oster ME. Association of Digoxin With Preserved Echocardiographic Indices in the Interstage Period: A Possible Mechanism to Explain Improved Survival?. J Am Heart Assoc. 2021 Dec 07;10(23):e021443. doi: 10.1161/JAHA.121.021443. Epub 2021 Dec 02. PMID: 34854311.
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Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.

HGG advances

Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, Bais AS, Klonowski J, de Bellaing AM, Saini A, Wang MX, Emerel L, Salamacha N, Wyman SK, Lee C, Sing Li H, Miron A, Zhang J, Xing J, McNamara DM, Fung E, Kirshbom P, Mahle W, Kochilas LK, He Y, Garg V, White P, McBride KL, Benson DW, Gleason TG, Mital S, Lo CW.
PMID: 34888534
HGG Adv. 2021 Jul 08;2(3). doi: 10.1016/j.xhgg.2021.100037. Epub 2021 Jul 29.

Bicuspid aortic valve (BAV) with ~1%-2% prevalence is the most common congenital heart defect (CHD). It frequently results in valve disease and aorta dilation and is a major cause of adult cardiac surgery. BAV is genetically linked to rare...

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Teekakirikul P, Zhu W, Gabriel GC, et al. Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG Adv. 2021;2(3)doi: 10.1016/j.xhgg.2021.100037.
Teekakirikul, P., Zhu, W., Gabriel, G. C., Young, C. B., Williams, K., Martin, L. J., Hill, J. C., Richards, T., Billaud, M., Phillippi, J. A., Wang, J., Wu, Y., Tan, T., Devine, W., Lin, J. H., Bais, A. S., Klonowski, J., de Bellaing, A. M., Saini, A., Wang, M. X., Emerel, L., Salamacha, N., Wyman, S. K., Lee, C., Sing Li, H., Miron, A., Zhang, J., Xing, J., McNamara, D. M., Fung, E., Kirshbom, P., Mahle, W., Kochilas, L. K., He, Y., Garg, V., White, P., McBride, K. L., Benson, D. W., Gleason, T. G., Mital, S., & Lo, C. W. (2021). Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG advances, 2(3), . https://doi.org/10.1016/j.xhgg.2021.100037
Teekakirikul, Polakit, et al. "Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease." HGG advances vol. 2,3 (2021). doi: https://doi.org/10.1016/j.xhgg.2021.100037
Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, Bais AS, Klonowski J, de Bellaing AM, Saini A, Wang MX, Emerel L, Salamacha N, Wyman SK, Lee C, Sing Li H, Miron A, Zhang J, Xing J, McNamara DM, Fung E, Kirshbom P, Mahle W, Kochilas LK, He Y, Garg V, White P, McBride KL, Benson DW, Gleason TG, Mital S, Lo CW. Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG Adv. 2021 Jul 08;2(3). doi: 10.1016/j.xhgg.2021.100037. Epub 2021 Jul 29. PMID: 34888534; PMCID: PMC8653519.
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Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome.

The Journal of pediatrics

Alam S, Claxton JS, Mortillo M, Sassis L, Kefala-Karli P, Silberbach M, Kochilas L, Wechsler SB.
PMID: 34450123
J Pediatr. 2021 Dec;239:187-192.e1. doi: 10.1016/j.jpeds.2021.08.034. Epub 2021 Aug 24.

OBJECTIVE: To evaluate long-term survival in patients with Turner syndrome after congenital heart surgery with a focus on left heart obstructive lesions (LHOLs).STUDY DESIGN: We queried the Pediatric Cardiac Care Consortium, a US-based registry of congenital heart surgery, for...

Cite
Alam S, Claxton JS, Mortillo M, et al. Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. J Pediatr. 2021;239:187-192.e1doi: 10.1016/j.jpeds.2021.08.034.
Alam, S., Claxton, J. S., Mortillo, M., Sassis, L., Kefala-Karli, P., Silberbach, M., Kochilas, L., & Wechsler, S. B. (2021). Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. The Journal of pediatrics, 239187-192.e1. https://doi.org/10.1016/j.jpeds.2021.08.034
Alam, Sabikha, et al. "Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome." The Journal of pediatrics vol. 239 (2021): 187-192.e1. doi: https://doi.org/10.1016/j.jpeds.2021.08.034
Alam S, Claxton JS, Mortillo M, Sassis L, Kefala-Karli P, Silberbach M, Kochilas L, Wechsler SB. Thirty-Year Survival after Cardiac Surgery for Patients with Turner Syndrome. J Pediatr. 2021 Dec;239:187-192.e1. doi: 10.1016/j.jpeds.2021.08.034. Epub 2021 Aug 24. PMID: 34450123; PMCID: PMC8626205.
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Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?.

The Annals of thoracic surgery

Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L.
PMID: 33359723
Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24.

BACKGROUND: Aortic valve replacement in young children is associated with technical difficulties and potential morbidity. In contrast to the versatile Ross operation, mechanical prostheses (MP) are uncommonly used.METHODS: We examined transplant-free survival and cardiac reoperation among 124 young children...

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Alsoufi B, Knight JH, St Louis J, et al. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2020;113(1):166-173doi: 10.1016/j.athoracsur.2020.12.014.
Alsoufi, B., Knight, J. H., St Louis, J., Raghuveer, G., & Kochilas, L. (2022). Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. The Annals of thoracic surgery, 113(1), 166-173. https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi, Bahaaldin, et al. "Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?." The Annals of thoracic surgery vol. 113,1 (2022): 166-173. doi: https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24. PMID: 33359723; PMCID: PMC8219808.
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Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?.

The Annals of thoracic surgery

Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L.
PMID: 33359723
Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24.

BACKGROUND: Aortic valve replacement in young children is associated with technical difficulties and potential morbidity. In contrast to the versatile Ross operation, mechanical prostheses (MP) are uncommonly used.METHODS: We examined transplant-free survival and cardiac reoperation among 124 young children...

Cite
Alsoufi B, Knight JH, St Louis J, et al. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2020;113(1):166-173doi: 10.1016/j.athoracsur.2020.12.014.
Alsoufi, B., Knight, J. H., St Louis, J., Raghuveer, G., & Kochilas, L. (2022). Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. The Annals of thoracic surgery, 113(1), 166-173. https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi, Bahaaldin, et al. "Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?." The Annals of thoracic surgery vol. 113,1 (2022): 166-173. doi: https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24. PMID: 33359723; PMCID: PMC8219808.
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Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?.

The Annals of thoracic surgery

Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L.
PMID: 33359723
Ann Thorac Surg. 2020 Dec 24; doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24.

BACKGROUND: Aortic valve replacement in young children is associated with technical difficulties and potential morbidity. In contrast to the versatile Ross operation, mechanical prostheses (MP) are uncommonly used.METHODS: We examined transplant-free survival and cardiac reoperation among 124 young children...

Cite
Alsoufi B, Knight JH, St Louis J, et al. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2020;doi: 10.1016/j.athoracsur.2020.12.014.
Alsoufi, B., Knight, J. H., St Louis, J., Raghuveer, G., & Kochilas, L. (2020). Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. The Annals of thoracic surgery, . https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi, Bahaaldin, et al. "Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?." The Annals of thoracic surgery vol. (2020). doi: https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2020 Dec 24; doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24. PMID: 33359723; PMCID: PMC8219808.
Copy Download .nbib Format: NLM
Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?.

The Annals of thoracic surgery

Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L.
PMID: 33359723
Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24.

BACKGROUND: Aortic valve replacement in young children is associated with technical difficulties and potential morbidity. In contrast to the versatile Ross operation, mechanical prostheses (MP) are uncommonly used.METHODS: We examined transplant-free survival and cardiac reoperation among 124 young children...

Cite
Alsoufi B, Knight JH, St Louis J, et al. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2020;113(1):166-173doi: 10.1016/j.athoracsur.2020.12.014.
Alsoufi, B., Knight, J. H., St Louis, J., Raghuveer, G., & Kochilas, L. (2022). Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. The Annals of thoracic surgery, 113(1), 166-173. https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi, Bahaaldin, et al. "Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?." The Annals of thoracic surgery vol. 113,1 (2022): 166-173. doi: https://doi.org/10.1016/j.athoracsur.2020.12.014
Alsoufi B, Knight JH, St Louis J, Raghuveer G, Kochilas L. Are Mechanical Prostheses Valid Alternatives to the Ross Procedure in Young Children Under 6 Years Old?. Ann Thorac Surg. 2022 Jan;113(1):166-173. doi: 10.1016/j.athoracsur.2020.12.014. Epub 2020 Dec 24. PMID: 33359723; PMCID: PMC8219808.
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Showing 1 to 12 of 20 entries