(Q41122400)

27 September 2017

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title

Hematologic disorders and nonimmune hydrops fetalis (English)

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27 September 2017

Arcasoy MO

1

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27 September 2017

Gallagher PG

series ordinal

2

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27 September 2017

language of work or name

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1 December 1995

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27 September 2017

published in

Seminars in Perinatology

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27 September 2017

volume

19

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27 September 2017

issue

6

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27 September 2017

page(s)

502-515

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Hydrops revisited: literature review of 1,414 cases published in the 1980s

27 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Investigation of nonimmune hydrops fetalis

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7 January 2021

Conditions associated with nonimmune hydrops fetalis.

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7 January 2021

Hydrops foetalis with a fast-moving haemoglobin.

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7 January 2021

Hydrops fetalis associated with Bart's hemoglobin in northern Thailand

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7 January 2021

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7 January 2021

Molecular defects in 2 examples of severe Hb H disease

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7 January 2021

Alpha thalassaemia in an Italian population

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7 January 2021

Frequency of alpha-thalassemia in Greece

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7 January 2021

Homozygous alpha-thalassaemia: clinical presentation, diagnosis and management. A review of 46 cases

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7 January 2021

Molecular characterization of severe alpha-thalassemias causing hydrops fetalis in Taiwan

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7 January 2021

Ultrasound measurement of placental thickness to detect pregnancies affected by homozygous alpha-thalassaemia-1

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7 January 2021

A simple sensitive prenatal test for hydrops fetalis caused by alpha-thalassaemia

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7 January 2021

Alpha-globin gene organisation and prenatal diagnosis of alpha-thalassaemia in Chinese

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7 January 2021

A PCR-based strategy to detect the common severe determinants of alpha thalassaemia

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7 January 2021

Carrier detection and prenatal diagnosis of alpha-thalassemia of Southeast Asian deletion by polymerase chain reaction

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7 January 2021

Survival of a hydropic infant with homozygous α-thalassemia-1

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7 January 2021

Normal long-term survival with alpha-thalassemia

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7 January 2021

Intrauterine therapy for homozygous alpha-thalassemia

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7 January 2021

Detection of the (--SEA) double alpha-globin gene deletion by a simple immunologic assay for embryonic zeta-globin chains

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7 January 2021

Fetal anaemia due to pyruvate kinase deficiency

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7 January 2021

Glucose phosphate isomerase deficiency as a cause of hydrops fetalis

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7 January 2021

Hydrops fetalis and stillbirth in a male glucose-6-phosphate dehydrogenase-deficient fetus possibly due to maternal ingestion of sulfisoxazole

1 reference

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7 January 2021

Hydrops fetalis associated with erythrocyte G-6-PD deficiency and maternal ingestion of fava beans and ascorbic acid

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7 January 2021

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene

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7 January 2021

Non-immune fetal hydrops with hepatic hemangioendothelioma and Kasabach-Merritt syndrome: a case report

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7 January 2021

Hydrops fetalis caused by fetal Kasabach-Merritt syndrome.

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7 January 2021

Nonimmune hydrops fetalis, hydramnios, microcephaly, and intracranial meningeal hemangioendothelioma

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7 January 2021

Fetomaternal hemorrhage. When to suspect, how to manage

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7 January 2021

Feto-maternal haemorrhage as a cause of fetal morbidity and mortality.

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7 January 2021

Successful treatment of hydrops fetalis caused by fetomaternal hemorrhage: a case report

1 reference

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7 January 2021

Comparison of predelivery versus postdelivery Kleihauer-Betke stains in cases of fetal death

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7 January 2021

Hydrops fetalis caused by massive maternofetal transplacental hemorrhage

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7 January 2021

Raised maternal serum-alpha-fetoprotein levels and spontaneous fetomaternal transfusion

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7 January 2021

Detection and measurement of fetomaternal haemorrhage: serum alpha-fetoprotein and the Kleihauer technique

1 reference

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7 January 2021

Nonimmune hydrops caused by massive fetomaternal hemorrhage and treated by intravascular transfusion

1 reference

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7 January 2021

Chronic, massive fetomaternal hemorrhage treated with repeated fetal intravascular transfusions

1 reference

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7 January 2021

Twin-twin transfusion syndrome: sonographic findings

1 reference

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7 January 2021

Fetal transfusion syndrome: antenatal factors predicting outcome

1 reference

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7 January 2021

Twin-to-twin transfusion syndrome: selective feticide by embolization of the hydropic fetus

1 reference

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7 January 2021

Twin transfusion syndrome: successful in utero treatment with digoxin

1 reference

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7 January 2021

Serial amniocenteses in the treatment of twin to twin transfusion complicated with acute polyhydramnios

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7 January 2021

Diagnosis and treatment of twin to twin transfusion in the mid-second trimester of pregnancy

1 reference

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7 January 2021

Clinical and echographic features of in utero cardiac dysfunction in the recipient twin in twin-twin transfusion syndrome

1 reference

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7 January 2021

Hydrops fetalis and in utero intracranial hemorrhage

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Nonimmune hydrops and hydrocephalus secondary to fetal intracranial hemorrhage

1 reference

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7 January 2021

Hydrops fetalis associated with small-bowel volvulus

1 reference

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7 January 2021

Diffuse neonatal haemangiomatosis with intra-uterine haemorrhage and hydrops fetalis: a case report

1 reference

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7 January 2021

Neonatal hepatic calcification in subcapsular haematoma with hydrops fetalis

1 reference

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7 January 2021

Prenatal diagnosis of acute non-lymphoblastic leukaemia in Down syndrome

1 reference

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7 January 2021

Prenatal diagnosis of transient myeloproliferative disorder via percutaneous umbilical blood sampling. Report of two cases in fetuses affected by Down's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Prenatally diagnosed non-immune hydrops caused by congenital transient leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Intrauterine diagnosis and management of transient myeloproliferative disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Congenital leukaemia: an unusual cause of stillbirth

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Perinatal visceral fibrosis accompanying the megakaryoblastic leukemoid reaction of Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Hydrops foetalis in 3 infants of a mother with acquired chronic pure red cell aplasia: transitory red cell aplasia in 1 of the infants

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

A congenital dyserythropoietic anaemia variant presenting as hydrops fetalis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

A variant congenital dyserythropoietic anaemia presenting as a fatal hydrops foetalis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2805%2980057-6

7 January 2021

10.1016/S0146-0005(05)80057-6

Identifiers

DOI

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27 September 2017

1 reference