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Heterodyne detection of multiply scattered monochromatic light with a multipixel detector

Optics letters, 2005-06, Vol.30 (11), p.1357

2005

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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Haematologica (Roma), 2014-09, Vol.99 (9), p.e168

2014

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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Nature genetics, 1996-06, Vol.13 (2), p.214-218

1996

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Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

Blood, 1997-06, Vol.89 (12), p.4628-4635

1997

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β Spectrin kissimmee : a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1

The Journal of clinical investigation, 1993-08, Vol.92 (2), p.612-616

1993

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Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

American journal of hematology, 1997-03, Vol.54 (3), p.242-248

1997

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Vitiligo in patients with metastatic melanoma: A good prognostic sign

Journal of the American Academy of Dermatology, 1983-11, Vol.9 (5), p.689-696

1983

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An Insertional Frameshift Mutation of the β-Spectrin Gene Associated With Elliptocytosis in Spectrin Nice (β220 216)

Blood, 1991-07, Vol.78 (2), p.517-523

1991

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Amino‐acid substitution in α‐spectrin commonly coinherited with nondominant hereditary spherocytosis

American journal of hematology, 1997-03, Vol.54 (3), p.233-241

1997

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Demographic study of clinically atypical (dysplastic) nevi in patients with melanoma and comparison subjects

Cancer research (Chicago, Ill.), 1985-04, Vol.45 (4), p.1855-1861

1985

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Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin

The New England journal of medicine, 1990-10, Vol.323 (15), p.1046-1050

1990

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A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis

British journal of haematology, 2000-12, Vol.111 (4), p.1190-1193

2000

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

The Journal of clinical investigation, 1995-03, Vol.95 (3), p.1174-1182

1995

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Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin αI/74-kilodalton tryptic peptide

Blood, 1991-09, Vol.78 (5), p.1364-1372

1991

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A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis

The Journal of clinical investigation, 1996-01, Vol.97 (2), p.373-380

1996

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G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene

Proceedings of the National Academy of Sciences - PNAS, 1984-08, Vol.81 (15), p.4894-4898

1984

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The pathophysiology and molecular genetics of beta thalassemia

The Mount Sinai journal of medicine, 1993-03, Vol.60 (2), p.95-103

FORGET, B. G

1993

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Pitfalls of genetic testing

The New England journal of medicine, 1996-10, Vol.335 (16), p.1236; author reply 1236-1236; author reply 1237

1996

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Familial polycythemia due to truncations of the erythropoietin receptor

Transactions of the American Clinical and Climatological Association, 2000, Vol.111, p.38-44; discussion 44-5

2000

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A prospective study of nosocomial-infection-related mortality assessed through mortality reviews in 14 hospitals in Northern France

The Journal of hospital infection, 2012-04, Vol.80 (4), p.310-315

2012

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Increased Expression of the Gγ and Aγ Globin Genes Associated With a Mutation in the Aγ Enhancer

Blood, 1994-06, Vol.83 (12), p.3727-3737

1994

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Release of pefloxacin bonded on catheters after intraperitoneal implantation in mice

Drugs (New York, N.Y.), 1995, Vol.49 Suppl 2 (Supplement 2), p.304-306

1995

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The thalassemias: molecular mechanisms of human genetic disease

American journal of human genetics, 1983-05, Vol.35 (3), p.333-361

1983

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Spectrin Jendouba : an αII/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site

Blood, 1992-08, Vol.80 (3), p.809-815

1992

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Hereditary pyropoikilocytosis and elliptocytosis in a white french family with the spectrin αI/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin αI domain

Blood, 1990-04, Vol.75 (8), p.1691-1698

1990

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Heterodyne detection of multiply scattered monochromatic light with a multipixel detector

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

β Spectrin kissimmee : a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

Vitiligo in patients with metastatic melanoma: A good prognostic sign

An Insertional Frameshift Mutation of the β-Spectrin Gene Associated With Elliptocytosis in Spectrin Nice (β220 216)

Amino‐acid substitution in α‐spectrin commonly coinherited with nondominant hereditary spherocytosis

Demographic study of clinically atypical (dysplastic) nevi in patients with melanoma and comparison subjects

Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin

A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis

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

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin αI/74-kilodalton tryptic peptide

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis

G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene

The pathophysiology and molecular genetics of beta thalassemia

Pitfalls of genetic testing

Familial polycythemia due to truncations of the erythropoietin receptor

A prospective study of nosocomial-infection-related mortality assessed through mortality reviews in 14 hospitals in Northern France

Increased Expression of the Gγ and Aγ Globin Genes Associated With a Mutation in the Aγ Enhancer

Release of pefloxacin bonded on catheters after intraperitoneal implantation in mice

The thalassemias: molecular mechanisms of human genetic disease

Spectrin Jendouba : an αII/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site

Hereditary pyropoikilocytosis and elliptocytosis in a white french family with the spectrin αI/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin αI domain

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