-
2
-
-
29144515527
-
Fetal OK-432 pleurodesis: Complete or incomplete? [2]
-
DOI 10.1002/uog.2634
-
Chen, M, JC Shih, BT Wang, et al: Fetal OK-432 pleurodesis: Complete or incomplete? Ultrasound Obstet. Gynecol. 26 (2005), 791-793. (Pubitemid 41810146)
-
(2005)
Ultrasound in Obstetrics and Gynecology
, vol.26
, Issue.7
, pp. 791-793
-
-
Chen, M.1
Shih, J.C.2
Wang, B.T.3
Chen, C.P.4
Yu, C.L.5
-
3
-
-
57349189618
-
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy
-
Ma, GC, CS Liu, SP Chang, et al: A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: Possible correlation with poor response to fetal therapy. Prenat. Diagn. 28 (2008), 1057-1063.
-
(2008)
Prenat. Diagn.
, vol.28
, pp. 1057-1063
-
-
Ma, G.C.1
Liu, C.S.2
Chang, S.P.3
-
4
-
-
34247552833
-
New treatment of early fetal chylothorax
-
Nygaard, U, K Sundberg, HS Nielsen, et al: New treatment of early fetal chylothorax. Obstet. Gynecol. 109 (2007), 1088-1092.
-
(2007)
Obstet. Gynecol.
, vol.109
, pp. 1088-1092
-
-
Nygaard, U.1
Sundberg, K.2
Nielsen, H.S.3
-
5
-
-
0036959853
-
Insights into the molecular pathogenesis and targeted treatment of lymphoedema
-
Sarristo, A, MJ Karkkainen, K Alitalo: Insights into the molecular pathogenesis and targeted treatment of lymphoedema. Ann. NY Acad. Sci. 979 (2002), 94-110.
-
(2002)
Ann. NY Acad. Sci.
, vol.979
, pp. 94-110
-
-
Sarristo, A.1
Karkkainen, M.J.2
Alitalo, K.3
-
6
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia, M, E Mehler, R Goldberg, et al: Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat. Genet. 29 (2001), 465-468.
-
(2001)
Nat. Genet.
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.2
Goldberg, R.3
-
7
-
-
57349108541
-
PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome
-
Ko, JM, JM Kim, JH Kim, et al: PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome. J. Hum. Genet. 53 (2008), 999-1006.
-
(2008)
J. Hum. Genet.
, vol.53
, pp. 999-1006
-
-
Ko, J.M.1
Kim, J.M.2
Kim, J.H.3
-
9
-
-
23244436779
-
Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites
-
Schluter, G, M Steckel, H Schiffmann, et al: Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites. Prenat. Diagn. 25 (2005), 574-576.
-
(2005)
Prenat. Diagn.
, vol.25
, pp. 574-576
-
-
Schluter, G.1
Steckel, M.2
Schiffmann, H.3
-
10
-
-
70350744524
-
PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings
-
Epub Aug 26
-
Lee, K, B Williams, K Roza, et al: PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings. Clin. Genet. 2008 Epub Aug 26
-
(2008)
Clin. Genet.
-
-
Lee, K.1
Williams, B.2
Roza, K.3
-
11
-
-
34347223262
-
Proinflammatory macrophage inhibition factor and interleukiun-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax
-
Chen, M, CY Hsieh, JC Shih, et al: Proinflammatory macrophage inhibition factor and interleukiun-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax. Prenat. Diagn. 27 (2007), 435-441.
-
(2007)
Prenat. Diagn.
, vol.27
, pp. 435-441
-
-
Chen, M.1
Hsieh, C.Y.2
Shih, J.C.3
-
12
-
-
10044263012
-
Thoracoamniotic shunting for fetal pleural effusions with hydrops
-
Picone, O, A Benachi, L Mandelbrot, et al: Thoracoamniotic shunting for fetal pleural effusions with hydrops. Am. J. Obstet. Gynecol. 191 (2004), 2047-2050.
-
(2004)
Am. J. Obstet. Gynecol.
, vol.191
, pp. 2047-2050
-
-
Picone, O.1
Benachi, A.2
Mandelbrot, L.3
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