(Q26852450)

Crossref

language of work or name

1 reference

December 2013

1 reference

Pediatric Clinics of North America

published in

1 reference

volume

60

1 reference

page(s)

1349-62

1 reference

issue

6

1 reference

Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Red cell membrane: past, present, and future

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

A Congenital Haemolytic Anaemia with Thermal Sensitivity of the Erythrocyte Membrane

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Spectrin-based skeleton in red blood cells and malaria

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Red cell membrane disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary red cell membrane disorders and laboratory diagnostic testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Red cell indices in classification and treatment of anemias: from M.M. Wintrobes's original 1934 classification to the third millennium

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Splenectomy for hereditary spherocytosis: complete, partial or not at all?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Contemporary pediatric splenectomy: continuing controversies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Partial splenectomy for hereditary spherocytosis: a multi-institutional review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Risks and benefits of splenectomy versus no splenectomy for hereditary spherocytosis--a personal view

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

28 September 2017

Hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Delayed adverse vascular events after splenectomy in hereditary spherocytosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary elliptocytosis: spectrin and protein 4.1R.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Update on the clinical spectrum and genetics of red blood cell membrane disorders.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: a case report and review of the literature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Prevalence of pulmonary hypertension in hereditary spherocytosis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary spherocytosis with leg ulcers healing after splenectomy

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Hereditary spherocytosis in neonates with hyperbilirubinemia.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Erythropoietin levels in the different clinical forms of hereditary spherocytosis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Laparoscopic splenectomy has become the gold standard in children.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4155395

Six cases of hereditary spherocytosis revealed by human parvovirus infection

28 November 2018

1 reference

12 December 2020

Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis

1 reference

12 December 2020

Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis

1 reference

12 December 2020

Deficiency of alpha-spectrin synthesis in burst-forming units-erythroid in lethal hereditary spherocytosis

1 reference

12 December 2020

Erythropoietin production and erythropoiesis in compensated and anaemic states of hereditary spherocytosis

1 reference

12 December 2020

Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity

1 reference

12 December 2020

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

1 reference

12 December 2020

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency

1 reference

12 December 2020

Screening for hereditary spherocytosis by use of automated erythrocyte indexes

1 reference

12 December 2020

Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency

1 reference

12 December 2020

High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis

1 reference

12 December 2020

Megaloblastic anaemia in congenital spherocytosis

1 reference

12 December 2020

Hematologic manifestations and diagnosis of parvovirus B19 infections

1 reference

12 December 2020

Compliance with immunizations in splenectomized individuals with hereditary spherocytosis

1 reference

12 December 2020

Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients

1 reference

12 December 2020

Extramedullary haematopoiesis secondary to hereditary spherocytosis

1 reference

12 December 2020

Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans

1 reference

12 December 2020

Red-blood-cell survival after splenectomy in congenital spherocytosis

1 reference

12 December 2020

Deficient red-cell spectrin in severe, recessively inherited spherocytosis

1 reference

12 December 2020

Partial spectrin deficiency in hereditary pyropoikilocytosis

1 reference

12 December 2020

Natural history of hereditary spherocytosis during the first year of life

1 reference

12 December 2020

Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in children

1 reference

12 December 2020

Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases

1 reference

12 December 2020