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Congenital heart disease in Down syndrome: an echocardiographic study.

Indian pediatrics

Bhatia S, Verma IC, Shrivastava S.
PMID: 1452307
Indian Pediatr. 1992 Sep;29(9):1113-6.

We evaluated the utility of echocardiography in assessing the frequency and nature of cardiac malformations in children with Down syndrome. Fifty cases of chromosomally proven Down syndrome were studied. A physical examination, electro cardiogram, radiograph of chest and two-dimensional...

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Bhatia S, Verma IC, Shrivastava S. Congenital heart disease in Down syndrome: an echocardiographic study. Indian Pediatr. 1992;29(9):1113-6
Bhatia, S., Verma, I. C., & Shrivastava, S. (1992). Congenital heart disease in Down syndrome: an echocardiographic study. Indian pediatrics, 29(9), 1113-6.
Bhatia, S, et al. "Congenital heart disease in Down syndrome: an echocardiographic study." Indian pediatrics vol. 29,9 (1992): 1113-6.
Bhatia S, Verma IC, Shrivastava S. Congenital heart disease in Down syndrome: an echocardiographic study. Indian Pediatr. 1992 Sep;29(9):1113-6. PMID: 1452307.
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[Familial congenital heart defects].

Sovetskoe zdravookhranenie Kirgizii

Akhunbaeva NI, Dzhumadilov ShD.
PMID: 4666419
Sov Zdravookhr Kirg. 1972 May-Jun;3:58-9.

No abstract available.

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Akhunbaeva NI, Dzhumadilov ShD. K voprosu o semeinykh vrezhdennykh porokakh serdtsa. [Familial congenital heart defects]. Sov Zdravookhr Kirg. 1972;3:58-9
Akhunbaeva, N. I., & Dzhumadilov, S. h. D. (1972). K voprosu o semeinykh vrezhdennykh porokakh serdtsa. [Familial congenital heart defects]. Sovetskoe zdravookhranenie Kirgizii, 358-9.
Akhunbaeva, N I, and Dzhumadilov, Sh D. "K voprosu o semeinykh vrezhdennykh porokakh serdtsa." [Familial congenital heart defects]. Sovetskoe zdravookhranenie Kirgizii vol. 3 (1972): 58-9.
Akhunbaeva NI, Dzhumadilov ShD. K voprosu o semeinykh vrezhdennykh porokakh serdtsa. [Familial congenital heart defects]. Sov Zdravookhr Kirg. 1972 May-Jun;3:58-9. Russian. PMID: 4666419.
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Genetics of congenital heart disease.

Current opinion in cardiology

Edwards JJ, Gelb BD.
PMID: 26872209
Curr Opin Cardiol. 2016 May;31(3):235-41. doi: 10.1097/HCO.0000000000000274.

PURPOSE OF REVIEW: The goal of this review is to highlight recent discoveries in the field of genetics as it relates to congenital heart disease (CHD). Recent advancements in next generation sequencing technology and tools to interpret this growing...

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Edwards JJ, Gelb BD. Genetics of congenital heart disease. Curr Opin Cardiol. 2016;31(3):235-41doi: 10.1097/HCO.0000000000000274.
Edwards, J. J., & Gelb, B. D. (2016). Genetics of congenital heart disease. Current opinion in cardiology, 31(3), 235-41. https://doi.org/10.1097/HCO.0000000000000274
Edwards, Jonathan J, and Gelb, Bruce D. "Genetics of congenital heart disease." Current opinion in cardiology vol. 31,3 (2016): 235-41. doi: https://doi.org/10.1097/HCO.0000000000000274
Edwards JJ, Gelb BD. Genetics of congenital heart disease. Curr Opin Cardiol. 2016 May;31(3):235-41. doi: 10.1097/HCO.0000000000000274. PMID: 26872209; PMCID: PMC4868504.
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Congenital heart disease as a familial occurrence.

Archives of pediatrics

JOHNSON JL.
PMID: 13790296
Arch Pediatr. 1961 Jul;78:253-68.

No abstract available.

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JOHNSON JL. Congenital heart disease as a familial occurrence. Arch Pediatr. 1961;78:253-68
JOHNSON, J. L. (1961). Congenital heart disease as a familial occurrence. Archives of pediatrics, 78253-68.
JOHNSON, J L. "Congenital heart disease as a familial occurrence." Archives of pediatrics vol. 78 (1961): 253-68.
JOHNSON JL. Congenital heart disease as a familial occurrence. Arch Pediatr. 1961 Jul;78:253-68. PMID: 13790296.
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[On the etiology of congenital heart defects; report of an observation on the frequent presence of congenital heart defects in a family].

Zeitschrift fur Kinderheilkunde

GUTHEIL H, BACHMANN K.
PMID: 13709982
Z Kinderheilkd. 1961;85:569-82.

No abstract available.

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GUTHEIL H, BACHMANN K. [On the etiology of congenital heart defects; report of an observation on the frequent presence of congenital heart defects in a family]. Z Kinderheilkd. 1961;85:569-82
GUTHEIL, H., & BACHMANN, K. (1961). [On the etiology of congenital heart defects; report of an observation on the frequent presence of congenital heart defects in a family]. Zeitschrift fur Kinderheilkunde, 85569-82.
GUTHEIL, H, and BACHMANN, K. "[On the etiology of congenital heart defects; report of an observation on the frequent presence of congenital heart defects in a family]." Zeitschrift fur Kinderheilkunde vol. 85 (1961): 569-82.
GUTHEIL H, BACHMANN K. [On the etiology of congenital heart defects; report of an observation on the frequent presence of congenital heart defects in a family]. Z Kinderheilkd. 1961;85:569-82. German. PMID: 13709982.
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Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease.

Circulation. Genomic and precision medicine

Paige SL, Saha P, Priest JR.
PMID: 29555674
Circ Genom Precis Med. 2018 Mar;11(3):e002097. doi: 10.1161/CIRCGEN.118.002097.

No abstract available.

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Paige SL, Saha P, Priest JR. Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease. Circ Genom Precis Med. 2018;11(3):e002097doi: 10.1161/CIRCGEN.118.002097.
Paige, S. L., Saha, P., & Priest, J. R. (2018). Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease. Circulation. Genomic and precision medicine, 11(3), e002097. https://doi.org/10.1161/CIRCGEN.118.002097
Paige, Sharon L, et al. "Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease." Circulation. Genomic and precision medicine vol. 11,3 (2018): e002097. doi: https://doi.org/10.1161/CIRCGEN.118.002097
Paige SL, Saha P, Priest JR. Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease. Circ Genom Precis Med. 2018 Mar;11(3):e002097. doi: 10.1161/CIRCGEN.118.002097. PMID: 29555674; PMCID: PMC6049807.
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[Etiology of congenital disease and thoracic surgery].

[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai

Takao A.
PMID: 4056494
Nihon Kyobu Geka Gakkai Zasshi. 1985 May;33(5):617-20.

No abstract available.

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Takao A. [Etiology of congenital disease and thoracic surgery]. Nihon Kyobu Geka Gakkai Zasshi. 1985;33(5):617-20
Takao, A. (1985). [Etiology of congenital disease and thoracic surgery]. [Zasshi] [Journal]. Nihon Kyobu Geka Gakkai, 33(5), 617-20.
Takao, A. "[Etiology of congenital disease and thoracic surgery]." [Zasshi] [Journal]. Nihon Kyobu Geka Gakkai vol. 33,5 (1985): 617-20.
Takao A. [Etiology of congenital disease and thoracic surgery]. Nihon Kyobu Geka Gakkai Zasshi. 1985 May;33(5):617-20. Japanese. PMID: 4056494.
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Evaluation of relatives for congenital heart defects.

The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society

Thurmon TF.
PMID: 8576632
J La State Med Soc. 1996 Jan;148(1):31-7.

Current and developing knowledge of mechanisms underlying the embryological development of congenital heart defects strongly suggests that medical evaluation should be extended to relatives of patients. Relatives may be found to have either subclinical or significant heart defects of...

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Thurmon TF. Evaluation of relatives for congenital heart defects. J La State Med Soc. 1996;148(1):31-7
Thurmon, T. F. (1996). Evaluation of relatives for congenital heart defects. The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society, 148(1), 31-7.
Thurmon, T F. "Evaluation of relatives for congenital heart defects." The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society vol. 148,1 (1996): 31-7.
Thurmon TF. Evaluation of relatives for congenital heart defects. J La State Med Soc. 1996 Jan;148(1):31-7. PMID: 8576632.
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[The genetics of congenital cardiopathies].

Revista clinica espanola

SANCHEZ CASCOS A.
PMID: 13746053
Rev Clin Esp. 1961 Jul 15;82:1-8.

No abstract available.

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SANCHEZ CASCOS A. [The genetics of congenital cardiopathies]. Rev Clin Esp. 1961;82:1-8
SANCHEZ CASCOS, A. (1961). [The genetics of congenital cardiopathies]. Revista clinica espanola, 821-8.
SANCHEZ CASCOS, A. "[The genetics of congenital cardiopathies]." Revista clinica espanola vol. 82 (1961): 1-8.
SANCHEZ CASCOS A. [The genetics of congenital cardiopathies]. Rev Clin Esp. 1961 Jul 15;82:1-8. Spanish. PMID: 13746053.
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[3 cases of familial congenital cardiac defect of the same type].

Grudnaia khirurgiia (Moscow, Russia)

Tashpulatov AT, Grents VG, Simakova AA.
PMID: 608605
Grudn Khir. 1977 Nov-Dec;(6):70-1.

No abstract available.

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Tashpulatov AT, Grents VG, Simakova AA. Tri sluchaia odnotipnogo semeĭnogo vrozhdennogo poroka serdtsa. [3 cases of familial congenital cardiac defect of the same type]. Grudn Khir. 1977;(6):70-1
Tashpulatov, A. T., Grents, V. G., & Simakova, A. A. (1977). Tri sluchaia odnotipnogo semeĭnogo vrozhdennogo poroka serdtsa. [3 cases of familial congenital cardiac defect of the same type]. Grudnaia khirurgiia (Moscow, Russia), (6), 70-1.
Tashpulatov, A T, et al. "Tri sluchaia odnotipnogo semeĭnogo vrozhdennogo poroka serdtsa." [3 cases of familial congenital cardiac defect of the same type]. Grudnaia khirurgiia (Moscow, Russia) vol. ,6 (1977): 70-1.
Tashpulatov AT, Grents VG, Simakova AA. Tri sluchaia odnotipnogo semeĭnogo vrozhdennogo poroka serdtsa. [3 cases of familial congenital cardiac defect of the same type]. Grudn Khir. 1977 Nov-Dec;(6):70-1. Russian. PMID: 608605.
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The National Heart, Lung, and Blood Institute bench to bassinet Program: a new paradigm for translational research.

Journal of the American College of Cardiology

Kaltman JR, Schramm C, Pearson GD.
PMID: 20298934
J Am Coll Cardiol. 2010 Mar 23;55(12):1262-1265. doi: 10.1016/j.jacc.2009.11.055.

No abstract available.

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Kaltman JR, Schramm C, Pearson GD. The National Heart, Lung, and Blood Institute bench to bassinet Program: a new paradigm for translational research. J Am Coll Cardiol. 2010;55(12):1262-1265doi: 10.1016/j.jacc.2009.11.055.
Kaltman, J. R., Schramm, C., & Pearson, G. D. (2010). The National Heart, Lung, and Blood Institute bench to bassinet Program: a new paradigm for translational research. Journal of the American College of Cardiology, 55(12), 1262-1265. https://doi.org/10.1016/j.jacc.2009.11.055
Kaltman, Jonathan R, et al. "The National Heart, Lung, and Blood Institute bench to bassinet Program: a new paradigm for translational research." Journal of the American College of Cardiology vol. 55,12 (2010): 1262-1265. doi: https://doi.org/10.1016/j.jacc.2009.11.055
Kaltman JR, Schramm C, Pearson GD. The National Heart, Lung, and Blood Institute bench to bassinet Program: a new paradigm for translational research. J Am Coll Cardiol. 2010 Mar 23;55(12):1262-1265. doi: 10.1016/j.jacc.2009.11.055. PMID: 20298934.
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[Pediatric cardiac disease: indications for family screening and risk stratification].

Praxis

Pfammatter JP.
PMID: 18770925
Praxis (Bern 1994). 2008 Jun 25;97(13):727-32. doi: 10.1024/1661-8157.97.13.727.

In some forms of cardiac disease in childhood, familial occurrence is frequent. This implies the question whether family members should undergo cardiologic screening examinations. For cardiomyopathies the familiarity is so frequent and morbidity so important that examination by echo...

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Pfammatter JP. Herzerkrankungen beim Kind: Indikationen zu Risikoabklärungen und Familienscreening. [Pediatric cardiac disease: indications for family screening and risk stratification]. Praxis (Bern 1994). 2008;97(13):727-32doi: 10.1024/1661-8157.97.13.727.
Pfammatter, J. P. (2008). Herzerkrankungen beim Kind: Indikationen zu Risikoabklärungen und Familienscreening. [Pediatric cardiac disease: indications for family screening and risk stratification]. Praxis, 97(13), 727-32. https://doi.org/10.1024/1661-8157.97.13.727
Pfammatter, Jean-Pierre. "Herzerkrankungen beim Kind: Indikationen zu Risikoabklärungen und Familienscreening." [Pediatric cardiac disease: indications for family screening and risk stratification]. Praxis vol. 97,13 (2008): 727-32. doi: https://doi.org/10.1024/1661-8157.97.13.727
Pfammatter JP. Herzerkrankungen beim Kind: Indikationen zu Risikoabklärungen und Familienscreening. [Pediatric cardiac disease: indications for family screening and risk stratification]. Praxis (Bern 1994). 2008 Jun 25;97(13):727-32. doi: 10.1024/1661-8157.97.13.727. German. PMID: 18770925.
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Showing 1 to 12 of 22 entries