-
1
-
-
0032817942
-
Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax
-
Puddy V, Lam BCC, Tang M, et al. Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax. Prenat Diagn 1999;19:764-766
-
(1999)
Prenat Diagn
, vol.19
, pp. 764-766
-
-
Puddy, V.1
Lam, B.C.C.2
Tang, M.3
-
2
-
-
0035209935
-
Chylothorax and respiratory distress in a newborn with trisomy 21
-
Turan O, Canter B, Ergenekon E, Koc E, Atalay Y. Chylothorax and respiratory distress in a newborn with trisomy 21. Eur J Pediatr 2001;160:744-745
-
(2001)
Eur J Pediatr
, vol.160
, pp. 744-745
-
-
Turan, O.1
Canter, B.2
Ergenekon, E.3
Koc, E.4
Atalay, Y.5
-
4
-
-
0022508402
-
Primary lymphatic dysplasia in children: Chylothorax, chylous ascites, and generalized lymphatic dysplasia
-
Smeltzer DM, Stickler GB, Fleming RE. Primary lymphatic dysplasia in children: chylothorax, chylous ascites, and generalized lymphatic dysplasia. Eur J Pediatr 1986;145:286-292
-
(1986)
Eur J Pediatr
, vol.145
, pp. 286-292
-
-
Smeltzer, D.M.1
Stickler, G.B.2
Fleming, R.E.3
-
5
-
-
0032846392
-
Pleuroperitoneal shunt in the management of chylothorax caused by thoracic lymphatic dysplasia
-
Podevin G, Levard G, Larroquet M, Gruner M. Pleuroperitoneal shunt in the management of chylothorax caused by thoracic lymphatic dysplasia. J Pediatr Surg 1999;34:1420-1422
-
(1999)
J Pediatr Surg
, vol.34
, pp. 1420-1422
-
-
Podevin, G.1
Levard, G.2
Larroquet, M.3
Gruner, M.4
-
6
-
-
0020047984
-
Experience with peritoneo-venous shunting for congenital chylous ascites in infants and children
-
Guttman FM, Montupet P, Bloss RS. Experience with peritoneo-venous shunting for congenital chylous ascites in infants and children. J Pediatr Surg 1982;17:368-372
-
(1982)
J Pediatr Surg
, vol.17
, pp. 368-372
-
-
Guttman, F.M.1
Montupet, P.2
Bloss, R.S.3
-
7
-
-
0021924416
-
The management of chylous ascites in children
-
Man DW, Spitz L. The management of chylous ascites in children. J Pediatr Surg 1985;20:72-75
-
(1985)
J Pediatr Surg
, vol.20
, pp. 72-75
-
-
Man, D.W.1
Spitz, L.2
-
8
-
-
0030981276
-
Lymphatic dysplasia in a neonate with Noonan's syndrome
-
Bloomfield F, Hadden W, Gunn TR. Lymphatic dysplasia in a neonate with Noonan's syndrome. Pediatr Radiol 1997;27:321-323
-
(1997)
Pediatr Radiol
, vol.27
, pp. 321-323
-
-
Bloomfield, F.1
Hadden, W.2
Gunn, T.R.3
-
10
-
-
0025642422
-
Congenital abnormalities of the lymphatic system: A new clinical classification
-
Hilliard RI, McKenobey JBJ, Phillips MJ. Congenital abnormalities of the lymphatic system: a new clinical classification. Pediatrics 1990;86:988-994
-
(1990)
Pediatrics
, vol.86
, pp. 988-994
-
-
Hilliard, R.I.1
McKenobey, J.B.J.2
Phillips, M.J.3
-
11
-
-
0346458751
-
Lymphatic vasculature development
-
Oliver G. Lymphatic vasculature development. Nat Rev Immunol 2004;4:35-45
-
(2004)
Nat Rev Immunol
, vol.4
, pp. 35-45
-
-
Oliver, G.1
-
12
-
-
0037428231
-
Lymphatics make the break
-
Jain RK, Padera TP. Lymphatics make the break. Science 2003;299:209-210
-
(2003)
Science
, vol.299
, pp. 209-210
-
-
Jain, R.K.1
Padera, T.P.2
-
13
-
-
0037428102
-
Regulation of blood and lymphatic vascular separation by signaling proteins SLP-76 and Syk
-
Abtahian F, Guerriero A, Sebzda E, et al. Regulation of blood and lymphatic vascular separation by signaling proteins SLP-76 and Syk. Science 2003;299:247-251
-
(2003)
Science
, vol.299
, pp. 247-251
-
-
Abtahian, F.1
Guerriero, A.2
Sebzda, E.3
-
14
-
-
0034041161
-
Missense mutation interfere with VEGFR-3 signaling in primary lymphoedema
-
Karkkainen M, Ferrel RE, Lawrence EC, et al. Missense mutation interfere with VEGFR-3 signaling in primary lymphoedema. Nat Genet 2000;25:153-159
-
(2000)
Nat Genet
, vol.25
, pp. 153-159
-
-
Karkkainen, M.1
Ferrel, R.E.2
Lawrence, E.C.3
-
15
-
-
0033646615
-
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
-
Fang J, Dagenais SL, Erickson RP, et al. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am J Hum Genet 2000;67:1382-1388
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1382-1388
-
-
Fang, J.1
Dagenais, S.L.2
Erickson, R.P.3
-
16
-
-
0018652055
-
Dysplasia of the lymphatics with lymphoedema, generalized lympangiectasis, chylothorax and "pseudo-storage-disease"
-
Heimpel H, Bierich JR, Herrmann JM, Meister H, Vollmar J. Dysplasia of the lymphatics with lymphoedema, generalized lympangiectasis, chylothorax and "pseudo-storage-disease". Lymphology 1979;12:228-240
-
(1979)
Lymphology
, vol.12
, pp. 228-240
-
-
Heimpel, H.1
Bierich, J.R.2
Herrmann, J.M.3
Meister, H.4
Vollmar, J.5
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