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Whipple's Disease and “Tropheryma whippelii”

Clinical Microbiology Reviews, 2001-07, Vol.14 (3), p.561-583

2001

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Detection of Tropheryma whipplei DNA in Feces by PCR Using a Target Capture Method

Journal of Clinical Microbiology, 2002-07, Vol.40 (7), p.2466-2471

2002

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Evaluation of a Specific Nested PCR Targeting Domain III of the 23S rRNA Gene of “Tropheryma whippelii” and Proposal of a Classification System for Its Molecular Variants

Journal of Clinical Microbiology, 2000-02, Vol.38 (2), p.595-599

2000

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A Woman with Missing Hb A 2 Due to a Novel (εγ)δβ 0 -Thalassemia and a Novel δ-Globin Variant Hb A 2 -Gebenstorf ( HBD : c.209G>A)

Hemoglobin, 2020-05, Vol.44 (3), p.214-217

2020

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Homogeneity of 16S-23S Ribosomal Intergenic Spacer Regions of Tropheryma whippelii in Swiss Patients with Whipple’s Disease

Journal of Clinical Microbiology, 1999-01, Vol.37 (1), p.152-156

1999

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A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Hemoglobin, 2020-05, Vol.44 (3), p.214-217

2020

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Two Novel α 2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2 : c.428A > T) and Severe ( HBA2 : c.342-345insCC) α -Thalassemia Phenotype

Hemoglobin, 2015-03, Vol.39 (2), p.144-146

2015

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Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

Hemoglobin, 2015-04, Vol.39 (2), p.144-146

2015

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Molecular Cloning and Differential Expression Patterns of Avian Glutamate Receptor mRNAs

Journal of neurochemistry, 1995-06, Vol.64 (6), p.2413-2426

1995

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A 65 bp duplication/insertion in exon II of the β-globin gene causing β0-thalassemia

Haematologica (Roma), 2007-03, Vol.92 (3)

2007

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A new (G)γ-globin variant causing low oxygen affinity: Hb F-Brugine/Feldkirch [(G)γ105(G7)Leu→His; HBG2: c.317T>A]

Hemoglobin, 2014, Vol.38 (2), p.84-87

2014

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A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]

Hemoglobin, 2014-04, Vol.38 (2), p.84-87

2014

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Cloning and Sequencing of a Part of the Heat Shock Protein 65 Gene (hsp65) of “Tropheryma whippelii” and Its Use for Detection of “T. whippelii” in Clinical Specimens by PCR

Journal of Clinical Microbiology, 2000-06, Vol.38 (6), p.2248-2253

2000

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A Swiss (εγδβ)0‐thalassemia patient with a novel 3‐Mb deletion associated with mild mental impairment

American journal of hematology, 2013-02, Vol.88 (2), p.158-159

2013

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Rapid detection of Mycoplasma pneumoniae in clinical samples by real-time PCR

Journal of microbiological methods, 2000-06, Vol.41 (1), p.45-51

2000

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Neonatal cyanosis due to a new (G)γ-globin variant causing low oxygen affinity: Hb F-Sarajevo [(G)γ102(G4)Asn→Thr, AAC>ACC]

Hemoglobin, 2012-01, Vol.36 (2), p.109-113

2012

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Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene

Hemoglobin, 2005, Vol.29 (2), p.151-154

2005

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Unequal Interchromosomal Rearrangements May Result in Elastin Gene Deletions Causing the Williams-Beuren syndrome

Human molecular genetics, 1996-12, Vol.5 (12), p.1893-1898

1996

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A 65 bp duplication/insertion in exon II of the {beta}-globin gene causing {beta}0-thalassemia

Haematologica (Roma), 2007-03, Vol.92 (3), p.423-424

2007

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Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels

Hemoglobin, 2012-04, Vol.36 (2), p.177-182

2012

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Deactivation of Macrophages with Interleukin-4 Is the Key to the Isolation of Tropheryma whippelii

The Journal of infectious diseases, 1997-09, Vol.176 (3), p.672-677

1997

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PCR-positive tests for Tropheryma whippelii in patients without Whipple's disease

The Lancet (British edition), 1999-06, Vol.353 (9171), p.2214-2214

1999

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α-Thalassemia Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)

Hemoglobin, 2009-12, Vol.33 (6), p.519-522

2009

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Cloning and Sequencing of a Part of the Heat Shock Protein 65 Gene (hsp65) of “Tropheryma whippelii” and Its Use for Detection of “T. whippelii” in Clinical Specimens by PCR

Journal of clinical microbiology, 2000, Vol.38 (6), p.2248-2253

2000

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Molecular characterization of Treponema pallidum subsp. pallidum in Switzerland and France with a new multilocus sequence typing scheme

Whipple's Disease and “Tropheryma whippelii”

Detection of Tropheryma whipplei DNA in Feces by PCR Using a Target Capture Method

Evaluation of a Specific Nested PCR Targeting Domain III of the 23S rRNA Gene of “Tropheryma whippelii” and Proposal of a Classification System for Its Molecular Variants

A Woman with Missing Hb A 2 Due to a Novel (εγ)δβ 0 -Thalassemia and a Novel δ-Globin Variant Hb A 2 -Gebenstorf ( HBD : c.209G>A)

Homogeneity of 16S-23S Ribosomal Intergenic Spacer Regions of Tropheryma whippelii in Swiss Patients with Whipple’s Disease

A Woman with Missing Hb A2 Due to a Novel (εγ)δβ0-Thalassemia and a Novel δ-Globin Variant Hb A2-Gebenstorf (HBD: c.209G>A)

Two Novel α 2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2 : c.428A > T) and Severe ( HBA2 : c.342-345insCC) α -Thalassemia Phenotype

Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

Molecular Cloning and Differential Expression Patterns of Avian Glutamate Receptor mRNAs

A 65 bp duplication/insertion in exon II of the β-globin gene causing β0-thalassemia

A new (G)γ-globin variant causing low oxygen affinity: Hb F-Brugine/Feldkirch [(G)γ105(G7)Leu→His; HBG2: c.317T>A]

A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Brugine/Feldkirch [Gγ105(G7)Leu→His; HBG2: c.317T>A]

Cloning and Sequencing of a Part of the Heat Shock Protein 65 Gene (hsp65) of “Tropheryma whippelii” and Its Use for Detection of “T. whippelii” in Clinical Specimens by PCR

A Swiss (εγδβ)0‐thalassemia patient with a novel 3‐Mb deletion associated with mild mental impairment

Rapid detection of Mycoplasma pneumoniae in clinical samples by real-time PCR

Neonatal cyanosis due to a new (G)γ-globin variant causing low oxygen affinity: Hb F-Sarajevo [(G)γ102(G4)Asn→Thr, AAC>ACC]

Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene

Unequal Interchromosomal Rearrangements May Result in Elastin Gene Deletions Causing the Williams-Beuren syndrome

A 65 bp duplication/insertion in exon II of the {beta}-globin gene causing {beta}0-thalassemia

Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels

Deactivation of Macrophages with Interleukin-4 Is the Key to the Isolation of Tropheryma whippelii

PCR-positive tests for Tropheryma whippelii in patients without Whipple's disease

α-Thalassemia Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)

Cloning and Sequencing of a Part of the Heat Shock Protein 65 Gene (hsp65) of “Tropheryma whippelii” and Its Use for Detection of “T. whippelii” in Clinical Specimens by PCR

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