Marie-france Delisle

Umbilical Cord Hemangioma with Significant Cord Edema.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: June 22, 2021

No. 373-Cervical Insufficiency and Cervical Cerclage.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: January 15, 2019

No 373 - Insuffisance cervicale et cerclage cervical.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: January 15, 2019

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD148+1T (RHD01EL.31).

Journal: Transfusion

Published: February 28, 2018

Insuffisance cervicale et cerclage cervical.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: January 09, 2017

The role of cerclage beyond 24 weeks of gestation.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: November 07, 2014

Association between gestational age at birth, antenatal corticosteroids, and outcomes at 5 years: multiple courses of antenatal corticosteroids for preterm birth study at 5 years of age (MACS-5).

Journal: BMC pregnancy and childbirth

Published: March 01, 2014

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

Journal: Journal of pediatric hematology/oncology

Published: November 02, 2011

Umbilical Cord Hemangioma with Significant Cord Edema.

Umbilical Cord Hemangioma with Significant Cord Edema.

No. 373-Cervical Insufficiency and Cervical Cerclage.

No. 373-Cervical Insufficiency and Cervical Cerclage.

No 373 - Insuffisance cervicale et cerclage cervical.

No 373 - Insuffisance cervicale et cerclage cervical.

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD148+1T (RHD01EL.31).

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD148+1T (RHD01EL.31).

Insuffisance cervicale et cerclage cervical.

Insuffisance cervicale et cerclage cervical.

The role of cerclage beyond 24 weeks of gestation.

The role of cerclage beyond 24 weeks of gestation.

Association between gestational age at birth, antenatal corticosteroids, and outcomes at 5 years: multiple courses of antenatal corticosteroids for preterm birth study at 5 years of age (MACS-5).

Association between gestational age at birth, antenatal corticosteroids, and outcomes at 5 years: multiple courses of antenatal corticosteroids for preterm birth study at 5 years of age (MACS-5).

Cervical insufficiency and cervical cerclage.

Cervical insufficiency and cervical cerclage.

Multiple courses of antenatal corticosteroids for preterm birth study: outcomes in children at 5 years of age (MACS-5).

Multiple courses of antenatal corticosteroids for preterm birth study: outcomes in children at 5 years of age (MACS-5).

Effect of antenatal corticosteroids on fetal growth and gestational age at birth.

Effect of antenatal corticosteroids on fetal growth and gestational age at birth.

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

Marie-france Delisle

Umbilical Cord Hemangioma with Significant Cord Edema.

Umbilical Cord Hemangioma with Significant Cord Edema.

No. 373-Cervical Insufficiency and Cervical Cerclage.

No. 373-Cervical Insufficiency and Cervical Cerclage.

No 373 - Insuffisance cervicale et cerclage cervical.

No 373 - Insuffisance cervicale et cerclage cervical.

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31).

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31).

Insuffisance cervicale et cerclage cervical.

Insuffisance cervicale et cerclage cervical.

The role of cerclage beyond 24 weeks of gestation.

The role of cerclage beyond 24 weeks of gestation.

Association between gestational age at birth, antenatal corticosteroids, and outcomes at 5 years: multiple courses of antenatal corticosteroids for preterm birth study at 5 years of age (MACS-5).

Association between gestational age at birth, antenatal corticosteroids, and outcomes at 5 years: multiple courses of antenatal corticosteroids for preterm birth study at 5 years of age (MACS-5).

Cervical insufficiency and cervical cerclage.

Cervical insufficiency and cervical cerclage.

Multiple courses of antenatal corticosteroids for preterm birth study: outcomes in children at 5 years of age (MACS-5).

Multiple courses of antenatal corticosteroids for preterm birth study: outcomes in children at 5 years of age (MACS-5).

Effect of antenatal corticosteroids on fetal growth and gestational age at birth.

Effect of antenatal corticosteroids on fetal growth and gestational age at birth.

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD148+1T (RHD01EL.31).

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD148+1T (RHD01EL.31).