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1 ases, such as bronchopulmonary dysplasia and congenital diaphragmatic hernia.
2 t in postnatal lung function in infants with congenital diaphragmatic hernia.
3 n the hypoplastic lung of the ovine model of congenital diaphragmatic hernia.
4 ung growth may improve the outcome of severe congenital diaphragmatic hernia.
5 rbidity rates in this cohort of fetuses with congenital diaphragmatic hernia.
6 was performed in 26 fetuses with unilateral congenital diaphragmatic hernia.
7 outcome in fetuses with isolated left-sided congenital diaphragmatic hernia.
8 atal extracorporeal membrane oxygenation and congenital diaphragmatic hernia.
9 ups, such as those with sickle cell disease, congenital diaphragmatic hernia and Eisenmenger syndrome
10 al cerebellar deficiency in association with congenital diaphragmatic hernia, and severe facial disfi
11 e first from a one-way radiological study of congenital diaphragmatic hernia, and the second from a t
13 Morbidity and mortality for neonates with congenital diaphragmatic hernia-associated pulmonary hyp
15 d pulmonary hypoplasia, and the fetuses with congenital diaphragmatic hernia, at least a portion of t
19 de GATA4 and SOX7 confer a high risk of both congenital diaphragmatic hernia (CDH) and cardiac defect
20 lungs of human fetuses with severe isolated congenital diaphragmatic hernia (CDH) and changes in tra
23 ation and lethality at birth, reminiscent of congenital diaphragmatic hernia (CDH) cases in humans.
24 ith hypoplastic lung disease associated with congenital diaphragmatic hernia (CDH) continue to suffer
25 that racial and ethnic minority infants with congenital diaphragmatic hernia (CDH) have poorer clinic
26 ed in developing lungs from rat fetuses with congenital diaphragmatic hernia (CDH) induced by materna
53 therapies on the highest risk patients with congenital diaphragmatic hernia (CDH), those with agenes
54 will be readily identifiable perinatally in congenital diaphragmatic hernia (CDH), where the typical
55 clin (PGI2) is a therapeutic option to treat congenital diaphragmatic hernia (CDH)-associated pulmona
61 e, commonly used therapy among patients with congenital diaphragmatic hernia (CDH); however, data to
63 c masses (ITM, n=15), tracheal occlusion for congenital diaphragmatic hernia (CDH, n=13), and resecti
65 ts in diaphragm development are the cause of congenital diaphragmatic hernias (CDHs), a common and of
66 trasonographic lung-head ratio in left-sided congenital diaphragmatic hernias evaluated before 27 wee
67 ciated with agenesis of the corpus callosum, congenital diaphragmatic hernia, facial dysmorphology, o
68 rganoids from AF and tracheal fluid cells of congenital diaphragmatic hernia fetuses, recapitulating
69 MR imaging was accurate for distinguishing congenital diaphragmatic hernia from CCAM and was useful
70 -trial was performed in prenatally diagnosed congenital diaphragmatic hernia infants (n = 171) born b
73 Rationale: Pulmonary hypoplasia secondary to congenital diaphragmatic hernia is characterized by redu
76 of gestation and that had severe, left-sided congenital diaphragmatic hernia (liver herniation and a
77 The MR imaging diagnoses were three cases of congenital diaphragmatic hernia, nine of CCAM, two of BP
79 nvolving bowel perforation, bowel resection, congenital diaphragmatic hernia, oesophageal atresia, an
80 d aid clinicians who encounter children with congenital diaphragmatic hernia on either a regular or i
81 This trial involving fetuses with moderate congenital diaphragmatic hernia on the left side did not
82 rying singleton fetuses with severe isolated congenital diaphragmatic hernia on the left side to FETO
83 g singleton fetuses with a moderate isolated congenital diaphragmatic hernia on the left side to FETO
84 severe pulmonary hypoplasia due to isolated congenital diaphragmatic hernia on the left side, but da
85 severe pulmonary hypoplasia due to isolated congenital diaphragmatic hernia on the left side, but da
87 d update any clinician treating infants with congenital diaphragmatic hernia regarding the latest dev
88 ave a better response, whereas patients with congenital diaphragmatic hernia, severe sepsis, and alve
89 prospectively collected patient data in the Congenital Diaphragmatic Hernia Study Group registry bet
91 471; median, $111566 [IQR, $91195-$139936]), congenital diaphragmatic hernia (WIQR, $43948; median, $
92 l extracorporeal membrane oxygenation and/or congenital diaphragmatic hernia with an intelligence quo
93 4-month-old girl 32 days after a repair of a congenital diaphragmatic hernia, with ultrasound signs o
94 outcome in all cases of isolated left-sided congenital diaphragmatic hernia without prenatal interve