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The molecular genetic approach to Bartter's syndrome

Journal of molecular medicine (Berlin, Germany), 1998-04, Vol.76 (5), p.317-325

1998

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Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome

American journal of human genetics, 1998-06, Vol.62 (6), p.1332-1340

1998

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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Kidney international, 1998-09, Vol.54 (3), p.720-730

1998

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Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function

Biochemical and biophysical research communications, 1997-01, Vol.230 (3), p.641-645

1997

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Algorithm for the identification of bacterial pathogens in positive blood cultures by real-time LightCycler polymerase chain reaction (PCR) with sequence-specific probes

Diagnostic microbiology and infectious disease, 2004-04, Vol.48 (4), p.229-241

2004

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Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome

Pediatric nephrology (Berlin, West), 1996-10, Vol.10 (5), p.551-554

1996

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Augmentation of fetal granulopoiesis with chorioamnionitis during the second trimester of gestation

Human pathology, 1994-03, Vol.25 (3), p.244-247

1994

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A common NKCC2 mutation in Costa Rican Bartter's syndrome patients : Evidence for a founder effect

Journal of the American Society of Nephrology, 1997-11, Vol.8 (11), p.1706-1711

1997

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Fetuses from preeclamptic mothers show reduced hepatic erythropoiesis

Pediatric research, 1998-03, Vol.43 (3), p.349-354

1998

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The molecular genetic approach to Bartter's syndrome

Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function

Algorithm for the identification of bacterial pathogens in positive blood cultures by real-time LightCycler polymerase chain reaction (PCR) with sequence-specific probes

Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome

Augmentation of fetal granulopoiesis with chorioamnionitis during the second trimester of gestation

A common NKCC2 mutation in Costa Rican Bartter's syndrome patients : Evidence for a founder effect

Fetuses from preeclamptic mothers show reduced hepatic erythropoiesis

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