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51

Comparative Effects of Aging Process on Phosphatidylcholine Biosynthesis Pathway: A Key Role for CTP-Phosphocholine Cytidylyltransferase?

J. M. LEPAGNOL, V. HEIDET

Journal:

Annals of the New York Academy of Sciences

Year:

1993

Language:

english

File:

PDF, 243 KB

english, 1993

52

Stem cell therapy for Alport syndrome: the hope beyond the hype

Gross, O., Borza, D.-B., Anders, H.-J., Licht, C., Weber, M., Segerer, S., Torra, R., Gubler, M.-C., Heidet, L., Harvey, S., Cosgrove, D., Lees, G., Kashtan, C., Gregory, M., Savige, J., Ding, J., Tho

Journal:

Nephrology Dialysis Transplantation

Year:

2008

Language:

english

File:

PDF, 303 KB

english, 2008

53

Ciliopathies A reference for clinicians

Heidet, L., Niaudet, P.

Journal:

Clinical Kidney Journal

Year:

2014

Language:

english

File:

PDF, 96 KB

english, 2014

54

Protéinurie et progression de la maladie rénale chronique : rôle du stress du réticulum endoplasmique et de Lcn2

El Karoui, K., Viau, A., Bienaimé, F., Heidet, L., Mollet, G., Knebelmann, B., Gallazzini, M., Terzi, F.

Journal:

Néphrologie & Thérapeutique

Year:

2014

Language:

french

File:

PDF, 72 KB

french, 2014

55

Proteolysis Breaks Tolerance toward Intact 345(IV) Collagen, Eliciting Novel Anti-Glomerular Basement Membrane Autoantibodies Specific for 345NC1 Hexamers

Olaru, F., Wang, X.-P., Luo, W., Ge, L., Miner, J. H., Kleinau, S., Geiger, X. J., Wasiluk, A., Heidet, L., Kitching, A. R., Borza, D.-B.

Journal:

The Journal of Immunology

Year:

2013

Language:

english

File:

PDF, 1.04 MB

english, 2013

56

Fetal serum α -1 microglobulin for renal function assessment: comparison with β 2-microglobulin and cystatin C

Nguyen, Claire, Dreux, Sophie, Heidet, Laurence, Czerkiewicz, Isabelle, Salomon, Laurent J., Guimiot, Fabien, Schmitz, Thomas, Tsatsaris, Vassilis, Boulot, Pierre, Rousseau, Thierry, Muller, Françoise

Journal:

Prenatal Diagnosis

Year:

2013

Language:

english

File:

PDF, 510 KB

english, 2013

57

Outcome following prenatal diagnosis of severe bilateral renal hypoplasia

Spaggiari, Emmanuel, Stirnemann, Julien J., Heidet, Laurence, Dreux, Sophie, Ville, Yves, Oury, Jean-Francois, Delezoide, Anne-Lise, Muller, Françoise

Journal:

Prenatal Diagnosis

Year:

2013

Language:

english

File:

PDF, 93 KB

english, 2013

58

Evidence of digenic inheritance in Alport syndrome

Mencarelli, M. A., Heidet, L., Storey, H., van Geel, M., Knebelmann, B., Fallerini, C., Miglietti, N., Antonucci, M. F., Cetta, F., Sayer, J. A., van den Wijngaard, A., Yau, S., Mari, F., Bruttini, M.

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 1.78 MB

english, 2015

59

A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes

Ratelade, J., Arrondel, C., Hamard, G., Garbay, S., Harvey, S., Biebuyck, N., Schulz, H., Hastie, N., Pontoglio, M., Gubler, M.-C., Antignac, C., Heidet, L.

Journal:

Human Molecular Genetics

Year:

2010

Language:

english

File:

PDF, 741 KB

english, 2010

60

Somatostatin Receptors in Brain and Pituitary

Epelbaum, J., Agid, F., Agid, Y., Beaudet, A., Bertrand, P., Enjalbert, A., Heidet, V., Kordon, C., Krantic, S., L&eacute, onard, J.F., Musset, F., Moyse, E., Peillon, F., Slama, A., Videau, C.

Journal:

Hormone Research

Year:

1989

File:

PDF, 1.24 MB

1989

61

Early Glomerular Filtration Defect and Severe Renal Disease in Podocin-Deficient Mice

Roselli, S., Heidet, L., Sich, M., Henger, A., Kretzler, M., Gubler, M.-C., Antignac, C.

Journal:

Molecular and Cellular Biology

Year:

2004

Language:

english

File:

PDF, 1.36 MB

english, 2004

62

The Alloantigenic Sites of 3 4 5(IV) Collagen: PATHOGENIC X-LINKED ALPORT ALLOANTIBODIES TARGET TWO ACCESSIBLE CONFORMATIONAL EPITOPES IN THE 5NC1 DOMAIN

Kang, J. S., Kashtan, C. E., Turner, A. N., Heidet, L., Hudson, B. G., Borza, D.-B.

Journal:

Journal of Biological Chemistry

Year:

2007

Language:

english

File:

PDF, 1.05 MB

english, 2007

63

« Kissing heart » : le collapsus ventriculaire échographique

Heidet, M., Barghout, M., Chossat, N.

Journal:

Annales françaises de médecine d'urgence

Year:

2015

Language:

french

File:

PDF, 119 KB

french, 2015

64

Phenotype and Outcome in Hereditary Tubulointerstitial Nephritis Secondary to UMOD Mutations

Bollee, G., Dahan, K., Flamant, M., Moriniere, V., Pawtowski, A., Heidet, L., Lacombe, D., Devuyst, O., Pirson, Y., Antignac, C., Knebelmann, B.

Journal:

Clinical Journal of the American Society of Nephrology

Year:

2011

Language:

english

File:

PDF, 777 KB

english, 2011

65

Hepatocyte nuclear factor 1 controls nephron tubular development

Massa, F., Garbay, S., Bouvier, R., Sugitani, Y., Noda, T., Gubler, M.-C., Heidet, L., Pontoglio, M., Fischer, E.

Journal:

Development (The Company of Biologists)

Year:

2013

Language:

english

File:

PDF, 5.56 MB

english, 2013

66

The Renal Lesions of Alport Syndrome

Heidet, L., Gubler, M.-C.

Journal:

Journal of the American Society of Nephrology

Year:

2009

Language:

english

File:

PDF, 481 KB

english, 2009

67

Deletions of both 5(IV) and 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours

Heidet, L., Dahan, K., Zhou, J., Xu, Z., Cochat, P., Gould, J. D. M., Leppig, K. A., Proesmans, W., Guyot, C., Guillot, M., Roussel, B., Tryggvason, K., Grunfeld, J.-P., Gubler, M.-C., Antignac, C.

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 749 KB

english, 1995

68

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

Temme, Johanna, Peters, Frederick, Lange, Katharina, Pirson, Yves, Heidet, Laurence, Torra, Roser, Grunfeld, Jean-Pierre, Weber, Manfred, Licht, Christoph, Müller, Gerhard-Anton, Gross, Oliver

Journal:

Kidney International

Year:

2012

Language:

english

File:

PDF, 247 KB

english, 2012

69

Murine Membranous Nephropathy: Immunization with 3(IV) Collagen Fragment Induces Subepithelial Immune Complexes and Fc R-Independent Nephrotic Syndrome

Zhang, J.-J., Malekpour, M., Luo, W., Ge, L., Olaru, F., Wang, X.-P., Bah, M., Sado, Y., Heidet, L., Kleinau, S., Fogo, A. B., Borza, D.-B.

Journal:

The Journal of Immunology

Year:

2012

Language:

english

File:

PDF, 1.74 MB

english, 2012

70

Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases

Heidet, L., Decramer, S., Pawtowski, A., Moriniere, V., Bandin, F., Knebelmann, B., Lebre, A. S., Faguer, S., Guigonis, V., Antignac, C., Salomon, R.

Journal:

Clinical Journal of the American Society of Nephrology

Year:

2010

Language:

english

File:

PDF, 155 KB

english, 2010

71

CO-58 – Syndrome néphrotique congénital: une étude multicentrique française

Berody, S., Salomon, R., Niaudet, P., Heidet, L., Baudouin, V., Boudaillez, B., de Parscau, L., Dunand, O., Flodrops, H., Fila, M., Garnier, A., Harambat, J., Louillet, F., Merieau, E., May, A., Pietr

Journal:

Archives de Pédiatrie

Year:

2015

Language:

french

File:

PDF, 68 KB

french, 2015

72

Endoplasmic reticulum stress drives proteinuria-induced kidney lesions via Lipocalin 2

El Karoui, Khalil, Viau, Amandine, Dellis, Olivier, Bagattin, Alessia, Nguyen, Clément, Baron, William, Burtin, Martine, Broueilh, Mélanie, Heidet, Laurence, Mollet, Géraldine, Druilhe, Anne, Antignac

Journal:

Nature Communications

Year:

2016

Language:

english

File:

PDF, 2.98 MB

english, 2016

73

Néphrocalcinose et mutations du gène NPT2c

Heidet, L., Biebuyck, N., Salomon, R., Reklaityte, D., Prié, D., Vargas-Poussou, R.

Journal:

Archives de Pédiatrie

Year:

2016

File:

PDF, 152 KB

2016

74

Le « Cakutome », un outil de séquençage haut-débit ciblé pour le diagnostic moléculaire et l’identification de nouveaux gènes impliqués dans les anomalies du développement des reins et des voies urinaires

Jeanpierre, C., Humbert, C., Morinière, V., Bole-Feysot, C., Nitschké, P., Fourrage, C., Salomon, R., Antignac, C., Heidet, L.

Journal:

Archives de Pédiatrie

Year:

2016

File:

PDF, 259 KB

2016

75

Syndrome d'Alport ou néphropathie héréditaire hématurique progressive avec surdité

Heidet, L., Gubler, M.-C.

Journal:

EMC - Pédiatrie - Maladies infectieuses

Year:

2010

Language:

french

File:

PDF, 1.07 MB

french, 2010

76

Human mutations affect the epigenetic/bookmarking function of HNF1B

Lerner, Jonathan, Bagattin, Alessia, Verdeguer, Francisco, Makinistoglu, Munevver P., Garbay, Serge, Felix, Tristan, Heidet, Laurence, Pontoglio, Marco

Journal:

Nucleic Acids Research

Year:

2016

Language:

english

File:

PDF, 9.21 MB

english, 2016

77

Syndrome d’Alport : néphropathie héréditaire associée à des mutations dans les gènes codant les chaînes de collagène de type IV

Heidet, L., Gubler, M.-C.

Journal:

EMC - Néphrologie

Year:

2013

Language:

french

File:

PDF, 1.55 MB

french, 2013

78

Syndrome d'Alport ou néphropathie héréditaire hématurique progressive avec surdité

Gubler, Marie-Claire, Heidet, Laurence, Antignac, Corinne

Journal:

EMC - Néphrologie

Year:

2006

Language:

french

File:

PDF, 198 KB

french, 2006

79

Hyperechogenic kidneys and polyhydramnios associated withHNF1Bgene mutation

Gondra, Leire, Décramer, Stéphane, Chalouhi, Gihad E., Muller, Françoise, Salomon, Rémi, Heidet, Laurence

Journal:

Pediatric Nephrology

Year:

2016

Language:

english

File:

PDF, 260 KB

english, 2016

80

Sequential fetal serum β2-microglobulin to predict postnatal renal function in bilateral or low urinary tract obstruction

Spaggiari, Emmanuel, Faure, Giuliana, Dreux, Sophie, Czerkiewicz, Isabelle, Stirnemann, Julien J., Guimiot, Fabien, Heidet, Laurence, Favre, Romain, Salomon, Laurent J., Oury, Jean François, Ville, Yv

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2016

Language:

english

File:

PDF, 1.19 MB

english, 2016

81

Impact of minor actinide recycling on sustainable fuel cycle options

Heidet, F., Kim, T.K., Taiwo, T.A.

Journal:

Nuclear Engineering and Design

Year:

2016

Language:

english

File:

PDF, 3.27 MB

english, 2016

82

Syndrome d’Alport : néphropathie héréditaire associée à des mutations dans les gènes codant les chaînes de collagène de type IV

Heidet, Laurence, Gubler, Marie-Claire

Journal:

Néphrologie & Thérapeutique

Year:

2016

File:

PDF, 1.40 MB

2016

83

Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical region

Heidet, L., Cohen-Solal, L., Boye, E., Thorner, P., Kemper, M.J., David, A., Piet, Larget, Zhou, J., Flinter, F., Zhang, X., Gubler, M.C, Antignac, C.

Journal:

Cytogenetic and Genome Research

Year:

1997

File:

PDF, 1.28 MB

1997

84

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

Heidet, Laurence, Morinière, Vincent, Henry, Charline, De Tomasi, Lara, Reilly, Madeline Louise, Humbert, Camille, Alibeu, Olivier, Fourrage, Cécile, Bole-Feysot, Christine, Nitschké, Patrick, Tores,

Journal:

Journal of the American Society of Nephrology

Year:

2017

File:

PDF, 860 KB

2017

85

Neutron Balance Analysis for Sustainability of Breed-and-Burn Reactors

Heidet, Florent, Greenspan, Ehud

Journal:

Nuclear Science and Engineering

Year:

2012

Language:

english

File:

PDF, 1.12 MB

english, 2012

86

Scene time interval in out-of-hospital cardiac arrest: It is time to measure time until patient contact

Heidet, Matthieu, Brami, Elise, Mermet, Éric, Vaux, Julien, Revaux, François, Chollet-Xémard, Charlotte, Lecarpentier, Eric, Da Cunha, Thierry, Marty, Jean

Journal:

The American Journal of Emergency Medicine

Year:

2017

Language:

english

File:

PDF, 744 KB

english, 2017

87

Cakutome, a high-throughput tool for molecular diagnosis and identification of novel causative genes for CAKUT patients

Heidet, L., Morinière, V., Henry, C., De Tomasi, L., Campait, R., Alibeu, O., Fourrage, C., Bole-Feysot, C., Nitschké, P., Pietrement, C., Gaillard, D., Gonzales, M., Novo, R., Schaeffer, E., Roume, J

Journal:

Archives de Pédiatrie

Year:

2017

Language:

english

File:

PDF, 146 KB

english, 2017

88

Treatment and outcome of congenital nephrotic syndrome

Bérody, Sandra, Heidet, Laurence, Gribouval, Olivier, Harambat, Jérome, Niaudet, Patrick, Baudouin, Veronique, Bacchetta, Justine, Boudaillez, Bernard, Dehennault, Maud, de Parscau, Loïc, Dunand, Oliv

Journal:

Nephrology Dialysis Transplantation

Year:

2018

Language:

english

File:

PDF, 366 KB

english, 2018

89

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group

Kashtan, Clifford E., Ding, Jie, Garosi, Guido, Heidet, Laurence, Massella, Laura, Nakanishi, Koichi, Nozu, Kandai, Renieri, Alessandra, Rheault, Michelle, Wang, Fang, Gross, Oliver

Journal:

Kidney International

Year:

2018

Language:

english

File:

PDF, 223 KB

english, 2018

90

OC05.02: Fetal urine biochemistry in prediction of long-term (10-30 years of age) postnatal renal function in posterior urethral valves

Dreux, S., Moussy-Durandy, A., Patin, F., Favre, R., Lortat-Jacob, S., Salomon, L.J., El Ghoneimi, A., Oury, J., Deschennes, G., Ville, Y., Heidet, L., Muller, F.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2017

Language:

english

File:

PDF, 43 KB

english, 2017

91

Prenatal hyperechogenic kidneys in three cases of infantile hypercalcemia associated with SLC34A1 mutations

Hureaux, Marguerite, Molin, Arnaud, Jay, Nadine, Saliou, Anne Hélène, Spaggiari, Emmanuel, Salomon, Rémi, Benachi, Alexandra, Vargas-Poussou, Rosa, Heidet, Laurence

Journal:

Pediatric Nephrology

Year:

2018

Language:

english

File:

PDF, 1.99 MB

english, 2018

92

FASt TEst Reactor (FASTER) design overview

Heidet, F., Grandy, C., Sumner, T., Belch, H., Brunett, A., Hill, R., Hoffman, E., Jin, E., Mohamed, W., Moisseytsev, A., Passerini, S., Sienicki, J., Vilim, R., Hayes, S.

Journal:

Progress in Nuclear Energy

Year:

2018

Language:

english

File:

PDF, 1.50 MB

english, 2018

93

Efficacy and tolerance of early administration of tranexamic acid in patients with cirrhosis presenting with acute upper gastrointestinal bleeding: a study protocol for a multicentre, randomised, double-blind, placebo-controlled trial (the EXARHOSE study)

Heidet, Matthieu, Amathieu, Roland, Audureau, Etienne, Augusto, Oriane, Nicolazo de Barmon, Violaine, Rialland, Amandine, Schmitz, David, Pierrang, François, Marty, Jean, Chollet-Xémard, Charlotte, Th

Journal:

Year:

2018

Language:

english

File:

PDF, 599 KB

english, 2018

94

Safety analysis of the FASt TEst reactor (FASTER) preconceptual design

Sumner, Tyler, Moisseytsev, Anton, Sienicki, James, Heidet, Florent

Journal:

Progress in Nuclear Energy

Year:

2018

Language:

english

File:

PDF, 1.22 MB

english, 2018

95

Core design and performance of the FASt TEst reactor (FASTER)

Heidet, F., Grandy, C., Hill, R.N.

Journal:

Progress in Nuclear Energy

Year:

2018

Language:

english

File:

PDF, 1.54 MB

english, 2018

96

OP11.09: Fetal cystoscopy versus vesicoamniotic shunting in lower urinary tract obstruction

Vinit, N., Gueneuc, A., Blanc, T., Bessières, B., Dreux, S., Heidet, L., Salomon, R., Lapillonne, A., Salomon, L.J., Spaggiari, E., Stirnemann, J., Ville, Y.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2018

Language:

english

File:

PDF, 47 KB

english, 2018

97

Thermal hydraulic model of the molten salt reactor experiment with the NEAMS system analysis module

Leandro, Adrian M., Heidet, Florent, Hu, Rui, Brown, Nicholas R.

Journal:

Annals of Nuclear Energy

Year:

2019

Language:

english

File:

PDF, 2.09 MB

english, 2019

98

Influenza vaccination among children with idiopathic nephrotic syndrome: an investigation of practices

Klifa, Roman, Toubiana, Julie, Michel, Alizée, Biebuyck, Nathalie, Charbit, Marina, Heidet, Laurence, Krid, Saoussen, Krug, Pauline, Salomon, Rémi, Boyer, Olivia

Journal:

Year:

2019

Language:

english

File:

PDF, 779 KB

english, 2019

99

Management and outcomes of cardiac arrests at nursing homes: A French nationwide cohort study

Vaux, Julien, Lecarpentier, Eric, Heidet, Matthieu, Oubaya, Nadia, Hubert, Hervé, Baert, Valentine, Segal, Nicolas, Mansouri, Nadia, Gueugniaud, Pierre-Yves, Bertrand, Catherine, Canoui-Poitrine, Flor

Journal:

Year:

2019

Language:

english

File:

PDF, 374 KB

english, 2019

100

School level of children carrying a HNF1B variant or a deletion

Laliève, Fanny, Decramer, Stéphane, Heidet, Laurence, Baudouin, Véronique, Lahoche, Annie, Llanas, Brigitte, Cochat, Pierre, Tenenbaum, Julie, Lavocat, Marie-Pierre, Eckart, Philippe, Broux, Françoise

Journal:

European Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 569 KB

english, 2019