(Q43833719)

27 November 2017

title

French retrospective multicentric study of neonatal hemochromatosis: importance of autopsy and autoimmune maternal manifestations (English)

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27 November 2017

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neonatal hemochromatosis

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11

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27 November 2017

Julien Baruteau

5

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author name string

Sophie Collardeau-Frachon

1

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27 November 2017

Sophie Heissat

2

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27 November 2017

Raymonde Bouvier

3

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27 November 2017

Monique Fabre

4

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27 November 2017

Pierre Broue

6

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27 November 2017

Marie-Pierre Cordier

7

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27 November 2017

Dominique Debray

8

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27 November 2017

Hanna Debiec

9

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27 November 2017

Pierre Ronco

10

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27 November 2017

language of work or name

English

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publication date

17 August 2012

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Pediatric and Developmental Pathology

27 November 2017

published in

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27 November 2017

volume

15

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27 November 2017

issue

6

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27 November 2017

page(s)

450-470

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Perinatal hemochromatosis: entity or end result?

27 November 2017

cites work

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Iron storage disease in parents and sibs of infants with neonatal hemochromatosis: 30-year follow-up

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Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosis

21 January 2018

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Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers

21 January 2018

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Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism

21 January 2018

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21 January 2018

Neonatal hemochromatosis

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Neonatal hemochromatosis: fetal liver disease leading to liver failure in the fetus and newborn

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Fetal and infantile hemochromatosis

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Neonatal hemochromatosis: a case report

21 January 2018

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Neonatal liver failure: a genetic and metabolic perspective.

21 January 2018

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High-dose immunoglobulin during pregnancy for recurrent neonatal haemochromatosis

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Neonatal hemochromatosis: is it an alloimmune disease?

21 January 2018

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Neonatal hemochromatosis: a congenital alloimmune hepatitis

21 January 2018

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Outcome of pregnancies at risk for neonatal hemochromatosis is improved by treatment with high-dose intravenous immunoglobulin.

21 January 2018

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Risks associated with the use of intravenous immunoglobulin

21 January 2018

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Non-invasive assessment of hepatic iron stores by MRI.

21 January 2018

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Oropharyngeal and upper respiratory tract mucosal-gland siderosis in neonatal hemochromatosis: an approach to biopsy diagnosis.

21 January 2018

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Minor salivary gland biopsy in neonatal hemochromatosis

21 January 2018

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Labial salivary gland involvement in neonatal hemochromatosis: a report of 2 cases and review of literature

21 January 2018

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Iron and pediatric liver disease

21 January 2018

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Inborn errors of metabolism in infancy: a guide to diagnosis

21 January 2018

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Neonatal liver failure: aetiologies and management--state of the art.

21 January 2018

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Cytomegalovirus infection, fetal liver disease, and neonatal hemochromatosis

21 January 2018

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SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect

21 January 2018

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Transaldolase deficiency: liver cirrhosis associated with a new inborn error in the pentose phosphate pathway

21 January 2018

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Transaldolase deficiency: a new cause of hydrops fetalis and neonatal multi-organ disease

21 January 2018

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Mitochondrial hepatopathies: advances in genetics and pathogenesis

21 January 2018

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Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency

21 January 2018

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Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

21 January 2018

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Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure

21 January 2018

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Severe perinatal liver disease and down syndrome: An apparent relationship

21 January 2018

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Neonatal haemochromatosis associated with Down syndrome

21 January 2018

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Incidence and clinical implications of GATA1 mutations in newborns with Down syndrome

21 January 2018

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Renal proximal tubular dysgenesis associated with severe neonatal hemosiderotic liver disease

21 January 2018

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Neonatal hemochromatosis, renal tubular dysgenesis, and hypocalvaria in a neonate.

21 January 2018

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Renal tubular dysgenesis and neonatal hemochromatosis without pulmonary hypoplasia.

21 January 2018

1 reference

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Villitis of unknown etiology: noninfectious chronic villitis in the placenta

21 January 2018

1 reference

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Chronic histiocytic intervillositis: a placental lesion associated with recurrent reproductive loss

21 January 2018

1 reference

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Hemophagocytic syndrome presenting as acute hepatic failure in two infants: clinical overlap with neonatal hemochromatosis

21 January 2018

1 reference

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Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children

21 January 2018

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Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports

21 January 2018

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Mechanisms of disease: Alloimmunization in renal diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F12-02-1155-OA.1

Alloimmune thrombocytopenia of the fetus and the newborn

21 January 2018

1 reference

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“Neonatal hemochromatosis”: A re-vision

21 January 2018

1 reference

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Vascular development and differentiation during human liver organogenesis

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.2350/12-02-1155-OA.1

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27 November 2017

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