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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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Lymphogranuloma venereum variant L2b-specific polymerase chain reaction: insertion used to close an epidemiological gap

Clinical microbiology and infection, 2011-11, Vol.17 (11), p.1727-1730

2011

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Analysis of 721 Chlamydia trachomatis-positive urogenital specimens from men and women using lymphogranuloma venereum L2-specific real-time PCR assay

Euro surveillance : bulletin européen sur les maladies transmissibles, 2006-10, Vol.11 (10), p.E061018.4-E061018.4

2006

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Tropheryma whippelii DNA in saliva of patients without Whipple's disease

Infection, 2000-07, Vol.28 (4), p.219-222

2000

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Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications

Journal of medical genetics, 2000-04, Vol.37 (4), p.281-286

2000

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Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

American journal of human genetics, 1996-11, Vol.59 (5), p.1114-1118

1996

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Rapid and reversible translocation of the catalytic subunit of cAMP‐dependent protein kinase type II from the Golgi complex to the nucleus

The EMBO journal, 1985-11, Vol.4 (11), p.2801-2806

1985

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Tandem triplication of chromosome 13q14 with inverted interstitial segment in a 4 year old girl

Journal of medical genetics, 2000-12, Vol.37 (12), p.964-967

2000

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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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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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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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Genetic variation in powdery mildew of barley: development of RAPD, SCAR, and VNTR markers

Phytopathology, 1994, Vol.84 (11), p.1316-1321

1994

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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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Neurons and astrocytes influence the development of purified o-2a progenitor cells

Glia, 1991, Vol.4 (6), p.559-571

1991

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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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Whipple endocarditis without overt gastrointestinal disease: report of four cases

Annals of internal medicine, 1999-07, Vol.131 (2), p.112

1999

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Philippinische Famile mit kombinierter alpha- und beta-Thalassämie

Zeitschrift für Geburtshilfe und Neonatologie, 2005, Vol.209 (S 2)

2005

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High Level of Unequal Meiotic Crossovers at the Origin of the 22q11.2 and 7q11.23 Deletions

Human molecular genetics, 1998-05, Vol.7 (5), p.887-894

1998

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Detection of three different types of 'Tropheryma whippelii' directly from clinical specimens by sequencing, single-strand conformation polymorphism (SSCP) analysis and type-specific PCR of their 16S-23S ribosomal intergenic spacer region

International journal of systematic and evolutionary microbiology, 1999-10, Vol.49 Pt 4 (4), p.1701-1706

1999

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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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Philippinische Familie mit kombinierter a- und b-Thalassämie

Swiss medical forum, 2004-09, Vol.4 (38)

2004

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Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation

European journal of human genetics : EJHG, 1998-03, Vol.6 (2), p.140-144

1998

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22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

Clinical genetics, 1998-01, Vol.53 (1), p.63-69

1998

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Whipple's Disease and “Tropheryma whippelii”

Lymphogranuloma venereum variant L2b-specific polymerase chain reaction: insertion used to close an epidemiological gap

Analysis of 721 Chlamydia trachomatis-positive urogenital specimens from men and women using lymphogranuloma venereum L2-specific real-time PCR assay

Tropheryma whippelii DNA in saliva of patients without Whipple's disease

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

Rapid and reversible translocation of the catalytic subunit of cAMP‐dependent protein kinase type II from the Golgi complex to the nucleus

Tandem triplication of chromosome 13q14 with inverted interstitial segment in a 4 year old girl

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

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

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

Genetic variation in powdery mildew of barley: development of RAPD, SCAR, and VNTR markers

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

Neurons and astrocytes influence the development of purified o-2a progenitor cells

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

Whipple endocarditis without overt gastrointestinal disease: report of four cases

Philippinische Famile mit kombinierter alpha- und beta-Thalassämie

High Level of Unequal Meiotic Crossovers at the Origin of the 22q11.2 and 7q11.23 Deletions

Detection of three different types of 'Tropheryma whippelii' directly from clinical specimens by sequencing, single-strand conformation polymorphism (SSCP) analysis and type-specific PCR of their 16S-23S ribosomal intergenic spacer region

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

Philippinische Familie mit kombinierter a- und b-Thalassämie

Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation

22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

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