-
1
-
-
16644383757
-
Conotruncal heart defects: Impact of genetic syndromes on immediate operative mortality
-
15554034
-
Anaclerio S, Di CV, Michielon G, Digilio MC, Formigari R, Picchio FM et al (2004) Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality. Ital Heart J 5:624-628
-
(2004)
Ital Heart J
, vol.5
, pp. 624-628
-
-
Anaclerio, S.1
Di, C.V.2
Michielon, G.3
Digilio, M.C.4
Formigari, R.5
Picchio, F.M.6
-
2
-
-
0038020123
-
Parathyroid function and growth in 22q11.2 deletion syndrome
-
12756381 10.1067/mpd.2003.156 1:CAS:528:DC%2BD3sXksVGlsrw%3D
-
Brauner R, de Le Harivel GA, Kindermans C, Le BJ, Prieur M, Lyonnet S et al (2003) Parathyroid function and growth in 22q11.2 deletion syndrome. J Pediatr 142:504-508
-
(2003)
J Pediatr
, vol.142
, pp. 504-508
-
-
Brauner, R.1
De Le Harivel, G.A.2
Kindermans, C.3
Le, B.J.4
Prieur, M.5
Lyonnet, S.6
-
3
-
-
0018415066
-
The spectrum of the DiGeorge syndrome
-
448529 10.1016/S0022-3476(79)80207-3 1:STN:280:DyaE1M7ps1alsw%3D%3D
-
Conley ME, Beckwith JB, Mancer JF, Tenckhoff L (1979) The spectrum of the DiGeorge syndrome. J Pediatr 94:883-890
-
(1979)
J Pediatr
, vol.94
, pp. 883-890
-
-
Conley, M.E.1
Beckwith, J.B.2
Mancer, J.F.3
Tenckhoff, L.4
-
4
-
-
0029873947
-
Latent hypoparathyroidism in children with conotruncal cardiac defects
-
8653876 1:STN:280:DyaK283gslOitg%3D%3D
-
Cuneo BF, Langman CB, Ilbawi MN, Ramakrishnan V, Cutilletta A, Driscoll DA (1996) Latent hypoparathyroidism in children with conotruncal cardiac defects. Circulation 93:1702-1708
-
(1996)
Circulation
, vol.93
, pp. 1702-1708
-
-
Cuneo, B.F.1
Langman, C.B.2
Ilbawi, M.N.3
Ramakrishnan, V.4
Cutilletta, A.5
Driscoll, D.A.6
-
5
-
-
0031046762
-
Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome
-
9066883 10.1002/(SICI)1096-8628(19970303)69:1<50: AID-AJMG10>3.0. CO;2-N 1:STN:280:DyaK2s3hvFGqsA%3D%3D
-
Cuneo BF, Driscoll DA, Gidding SS, Langman CB (1997) Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome. Am J Med Genet 69:50-55
-
(1997)
Am J Med Genet
, vol.69
, pp. 50-55
-
-
Cuneo, B.F.1
Driscoll, D.A.2
Gidding, S.S.3
Langman, C.B.4
-
6
-
-
77954710591
-
Course of ionized calcium after thyroidectomy
-
10.1007/s00268-010-0415-6
-
de Andrade SA, Salles JM, Soares JM, de Moraes GM, Carvalho JR, Rocha PR (2010) Course of ionized calcium after thyroidectomy. World J Surg 34:987-992
-
(2010)
World J Surg
, vol.34
, pp. 987-992
-
-
De Andrade, S.A.1
Salles, J.M.2
Soares, J.M.3
De Moraes, G.M.4
Carvalho, J.R.5
Rocha, P.R.6
-
7
-
-
0000025287
-
Discussions on a new concept of the cellular basis of immunity
-
10.1016/S0022-3476(65)81796-6
-
DiGeorge AM (1965) Discussions on a new concept of the cellular basis of immunity. J Pediatr 67:907-908
-
(1965)
J Pediatr
, vol.67
, pp. 907-908
-
-
Digeorge, A.M.1
-
8
-
-
0033033492
-
The Philadelphia story: The 22q11.2 deletion: Report on 250 patients
-
Donald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M et al (1999) The Philadelphia story: the 22q11.2 deletion: report on 250 patients. Genet Couns 10:11-24
-
(1999)
Genet Couns
, vol.10
, pp. 11-24
-
-
Donald-Mcginn, D.M.1
Kirschner, R.2
Goldmuntz, E.3
Sullivan, K.4
Eicher, P.5
Gerdes, M.6
-
9
-
-
34248373298
-
Increased calcium supplementation is associated with morbidity and mortality in the infant postoperative cardiac patient
-
17417127 10.1097/01.PCC.0000260784.30919.9E
-
Dyke PC, Yates AR, Cua CL, Hoffman TM, Hayes J, Feltes TF et al (2007) Increased calcium supplementation is associated with morbidity and mortality in the infant postoperative cardiac patient. Pediatr Crit Care Med 8:254-257
-
(2007)
Pediatr Crit Care Med
, vol.8
, pp. 254-257
-
-
Dyke, P.C.1
Yates, A.R.2
Cua, C.L.3
Hoffman, T.M.4
Hayes, J.5
Feltes, T.F.6
-
10
-
-
62149141331
-
Genetic syndromes and congenital heart defects: How is surgical management affected?
-
19091590 10.1016/j.ejcts.2008.11.005
-
Formigari R, Michielon G, Digilio MC, Piacentini G, Carotti A, Giardini A et al (2009) Genetic syndromes and congenital heart defects: How is surgical management affected? Eur J Cardiothorac Surg 35:606-614
-
(2009)
Eur J Cardiothorac Surg
, vol.35
, pp. 606-614
-
-
Formigari, R.1
Michielon, G.2
Digilio, M.C.3
Piacentini, G.4
Carotti, A.5
Giardini, A.6
-
11
-
-
0031671548
-
A population study of chromosome 22q11 deletions in infancy
-
9875047 10.1136/adc.79.4.348 1:STN:280:DyaK1M%2Fpt1ajtA%3D%3D
-
Goodship J, Cross I, LiLing J, Wren C (1998) A population study of chromosome 22q11 deletions in infancy. Arch Dis Child 79:348-351
-
(1998)
Arch Dis Child
, vol.79
, pp. 348-351
-
-
Goodship, J.1
Cross, I.2
Liling, J.3
Wren, C.4
-
12
-
-
63849233476
-
Introduction - Databases and the assessment of complications associated with the treatment of patients with congenital cardiac disease
-
Jacobs JP (2008) Introduction - databases and the assessment of complications associated with the treatment of patients with congenital cardiac disease. Cardiol Young 18(Suppl 2):1-37
-
(2008)
Cardiol Young
, vol.18
, Issue.SUPPL. 2
, pp. 1-37
-
-
Jacobs, J.P.1
-
13
-
-
40949146142
-
Parathyroid hormone reserve in 22q11.2 deletion syndrome
-
18344713 10.1097/GIM.0b013e3181634edf 1:CAS:528:DC%2BD1cXjt1Cqsb0%3D
-
Kapadia CR, Kim YE, Donald-McGinn DM, Zackai EH, Katz LE (2008) Parathyroid hormone reserve in 22q11.2 deletion syndrome. Genet Med 10:224-228
-
(2008)
Genet Med
, vol.10
, pp. 224-228
-
-
Kapadia, C.R.1
Kim, Y.E.2
Donald-Mcginn, D.M.3
Zackai, E.H.4
Katz, L.E.5
-
14
-
-
35348822545
-
Velocardiofacial syndrome, DiGeorge syndrome: The chromosome 22q11.2 deletion syndromes
-
17950858 10.1016/S0140-6736(07)61601-8 1:CAS:528:DC%2BD2sXhtF2hu7rM
-
Kobrynski LJ, Sullivan KE (2007) Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet 370:1443-1452
-
(2007)
Lancet
, vol.370
, pp. 1443-1452
-
-
Kobrynski, L.J.1
Sullivan, K.E.2
-
15
-
-
6344233335
-
A case of chromosome 22q11 deletion syndrome diagnosed in a 32-year-old man with hypoparathyroidism
-
15472168 10.1210/jc.2004-0442 1:CAS:528:DC%2BD2cXovVenur8%3D
-
Maalouf NM, Sakhaee K, Odvina CV (2004) A case of chromosome 22q11 deletion syndrome diagnosed in a 32-year-old man with hypoparathyroidism. J Clin Endocrinol Metab 89:4817-4820
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 4817-4820
-
-
Maalouf, N.M.1
Sakhaee, K.2
Odvina, C.V.3
-
16
-
-
32644487801
-
Genetic syndromes and outcome after surgical correction of tetralogy of Fallot
-
16488703 10.1016/j.athoracsur.2005.09.033
-
Michielon G, Marino B, Formigari R, Gargiulo G, Picchio F, Digilio MC et al (2006) Genetic syndromes and outcome after surgical correction of tetralogy of Fallot. Ann Thorac Surg 81:968-975
-
(2006)
Ann Thorac Surg
, vol.81
, pp. 968-975
-
-
Michielon, G.1
Marino, B.2
Formigari, R.3
Gargiulo, G.4
Picchio, F.5
Digilio, M.C.6
-
17
-
-
53749096268
-
Hypocalcemia in a patient with osteosarcoma and 22q11.2 deletion syndrome
-
18799940 10.1097/MPH.0b013e318168f072
-
Mussai FJ, Cunningham LC, Rezvani G, Stratakis CA, Reynolds JC, Nesterova G et al (2008) Hypocalcemia in a patient with osteosarcoma and 22q11.2 deletion syndrome. J Pediatr Hematol Oncol 30:612-617
-
(2008)
J Pediatr Hematol Oncol
, vol.30
, pp. 612-617
-
-
Mussai, F.J.1
Cunningham, L.C.2
Rezvani, G.3
Stratakis, C.A.4
Reynolds, J.C.5
Nesterova, G.6
-
18
-
-
0034681927
-
Early and intermediate outcomes after repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: Experience with 85 patients
-
10769284 1:STN:280:DC%2BD3c3jtlyisQ%3D%3D
-
Reddy VM, McElhinney DB, Amin Z, Moore P, Parry AJ, Teitel DF et al (2000) Early and intermediate outcomes after repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: experience with 85 patients. Circulation 101:1826-1832
-
(2000)
Circulation
, vol.101
, pp. 1826-1832
-
-
Reddy, V.M.1
McElhinney, D.B.2
Amin, Z.3
Moore, P.4
Parry, A.J.5
Teitel, D.F.6
-
19
-
-
0025985718
-
Normal parathyroid hormone responses to hypocalcemia during cardiopulmonary bypass
-
2064059 10.1097/00000542-199107000-00008 1:STN:280:DyaK3M3ptVehtQ%3D%3D
-
Robertie PG, Butterworth JF, Royster RL, Prielipp RC, Dudas L, Black KW et al (1991) Normal parathyroid hormone responses to hypocalcemia during cardiopulmonary bypass. Anesthesiology 75:43-48
-
(1991)
Anesthesiology
, vol.75
, pp. 43-48
-
-
Robertie, P.G.1
Butterworth, J.F.2
Royster, R.L.3
Prielipp, R.C.4
Dudas, L.5
Black, K.W.6
-
20
-
-
16944364802
-
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
-
9350810 10.1136/jmg.34.10.798 1:STN:280:DyaK1c%2FhtVaqsQ%3D%3D
-
Ryan AK, Goodship JA, Wilson DI, Philip N, Levy A, Seidel H et al (1997) Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 34:798-804
-
(1997)
J Med Genet
, vol.34
, pp. 798-804
-
-
Ryan, A.K.1
Goodship, J.A.2
Wilson, D.I.3
Philip, N.4
Levy, A.5
Seidel, H.6
-
21
-
-
0038697384
-
Hypoparathyroidism and 22q11 deletion syndrome
-
12765920 10.1136/adc.88.6.520 1:STN:280:DC%2BD3s3ktlahtw%3D%3D
-
Taylor SC, Morris G, Wilson D, Davies SJ, Gregory JW (2003) Hypoparathyroidism and 22q11 deletion syndrome. Arch Dis Child 88:520-522
-
(2003)
Arch Dis Child
, vol.88
, pp. 520-522
-
-
Taylor, S.C.1
Morris, G.2
Wilson, D.3
Davies, S.J.4
Gregory, J.W.5
-
22
-
-
64049086821
-
A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations
-
19145597 10.1002/elps.200800321 1:CAS:528:DC%2BD1MXjsFKit78%3D
-
Yang C, Shen L, Xu Z, Wu X, Mo X, Zhang J, Wang D et al (2009) A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations. Electrophoresis 30:465-471
-
(2009)
Electrophoresis
, vol.30
, pp. 465-471
-
-
Yang, C.1
Shen, L.2
Xu, Z.3
Wu, X.4
Mo, X.5
Zhang, J.6
Wang, D.7
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