PubMed

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.

Osbak KK, Colclough K, Saint-Martin C, Beer NL, Bellanné-Chantelot C, Ellard S, Gloyn AL.

Hum Mutat. 2009 Nov;30(11):1512-26.PMID: 19790256 [PubMed - in process]Related articles

HNF1B-related diabetes triggered by renal transplantation.

Zuber J, Bellanné-Chantelot C, Carette C, Canaud G, Gobrecht S, Gaha K, Mallet V, Martinez F, Thervet E, Timsit J, Legendre C, Dubois-Laforgue D.

Nat Rev Nephrol. 2009 Aug;5(8):480-4.PMID: 19639018 [PubMed - indexed for MEDLINE]Related articles

Analysis of the ten-eleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms.

Saint-Martin C, Leroy G, Delhommeau F, Panelatti G, Dupont S, James C, Plo I, Bordessoule D, Chomienne C, Delannoy A, Devidas A, Gardembas-Pain M, Isnard F, Plumelle Y, Bernard O, Vainchenker W, Najman A, Bellanné-Chantelot C; French Group of Familial Myeloproliferative Disorders.

Blood. 2009 Aug 20;114(8):1628-32. Epub 2009 Jun 29.PMID: 19564637 [PubMed - indexed for MEDLINE]Related articles

Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.

Lorini R, Klersy C, d'Annunzio G, Massa O, Minuto N, Iafusco D, Bellannè-Chantelot C, Frongia AP, Toni S, Meschi F, Cerutti F, Barbetti F; Italian Society of Pediatric Endocrinology and Diabetology (ISPED) Study Group.

Diabetes Care. 2009 Oct;32(10):1864-6. Epub 2009 Jun 29.PMID: 19564454 [PubMed - in process]Related articles

The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.

Laloi-Michelin M, Meas T, Ambonville C, Bellanné-Chantelot C, Beaufils S, Massin P, Vialettes B, Gin H, Timsit J, Bauduceau B, Bernard L, Bertin E, Blickle JF, Cahen-Varsaux J, Cailleba A, Casanova S, Cathebras P, Charpentier G, Chedin P, Crea T, Delemer B, Dubois-Laforgue D, Duchemin F, Ducluzeau PH, Bouhanick B, Dusselier L, Gabreau T, Grimaldi A, Guerci B, Jacquin V, Kaloustian E, Larger E, Lecleire-Collet A, Lorenzini F, Louis J, Mausset J, Murat A, Nadler-Fluteau S, Olivier F, Paquis-Flucklinger V, Paris-Bockel D, Raynaud I, Reznik Y, Riveline JP, Schneebeli S, Sonnet E, Sola-Gazagnes A, Thomas JL, Trabulsi B, Virally M, Guillausseau PJ; Mitochondrial Diabetes French Study Group.

J Clin Endocrinol Metab. 2009 Aug;94(8):3025-30. Epub 2009 May 26.PMID: 19470619 [PubMed - indexed for MEDLINE]Related articles

Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes.

Hartemann-Heurtier A, Simon A, Bellanné-Chantelot C, Reynaud R, Cavé H, Polak M, Vaxillaire M, Grimaldi A.

Diabetes Metab. 2009 Jun;35(3):233-5. Epub 2009 Apr 1.PMID: 19342262 [PubMed - indexed for MEDLINE]Related articles

Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction.

Bonnefond A, Bouatia-Naji N, Simon A, Saint-Martin C, Dechaume A, de Lonlay P, Polak M, Bellanné-Chantelot C, Froguel P, Vaxillaire M.

Diabetologia. 2009 May;52(5):982-5. Epub 2009 Feb 24. No abstract available. PMID: 19238352 [PubMed - indexed for MEDLINE]Related articles

Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.

Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Tardy V, Billaud L, Laborde K, Coussieu C, Morel Y, Vaury C, Golmard JL, Claustre A, Mornet E, Chakhtoura Z, Mowszowicz I, Bachelot A, Touraine P, Kuttenn F.

J Clin Endocrinol Metab. 2009 May;94(5):1570-8. Epub 2009 Feb 10.PMID: 19208730 [PubMed - indexed for MEDLINE]Related articles

Comparison of performances of various HbA1c methods in Haemoglobin Camperdown variant detection: consequences in diabetes management.

Gaborit B, Nicolay A, Valéro R, Bégu A, Badens C, Bellanné-Chantelot C, Portugal H, Vialettes B.

Clin Chim Acta. 2009 May;403(1-2):262-3. Epub 2009 Jan 9. No abstract available. Erratum in: Clin Chim Acta. 2009 Jul;405(1-2):163. PMID: 19168040 [PubMed - indexed for MEDLINE]Related articles

A syndrome with congenital neutropenia and mutations in G6PC3.

Boztug K, Appaswamy G, Ashikov A, Schäffer AA, Salzer U, Diestelhorst J, Germeshausen M, Brandes G, Lee-Gossler J, Noyan F, Gatzke AK, Minkov M, Greil J, Kratz C, Petropoulou T, Pellier I, Bellanné-Chantelot C, Rezaei N, Mönkemöller K, Irani-Hakimeh N, Bakker H, Gerardy-Schahn R, Zeidler C, Grimbacher B, Welte K, Klein C.

N Engl J Med. 2009 Jan 1;360(1):32-43.PMID: 19118303 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion.

González-Barroso MM, Giurgea I, Bouillaud F, Anedda A, Bellanné-Chantelot C, Hubert L, de Keyzer Y, de Lonlay P, Ricquier D.

PLoS One. 2008;3(12):e3850. Epub 2008 Dec 9.PMID: 19065272 [PubMed - indexed for MEDLINE]Related articlesFree article

Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism.

Damaj L, le Lorch M, Verkarre V, Werl C, Hubert L, Nihoul-Fékété C, Aigrain Y, de Keyzer Y, Romana SP, Bellanne-Chantelot C, de Lonlay P, Jaubert F.

J Clin Endocrinol Metab. 2008 Dec;93(12):4941-7. Epub 2008 Sep 16.PMID: 18796520 [PubMed - indexed for MEDLINE]Related articles

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.

Flanagan SE, Clauin S, Bellanné-Chantelot C, de Lonlay P, Harries LW, Gloyn AL, Ellard S.

Hum Mutat. 2009 Feb;30(2):170-80. Review.PMID: 18767144 [PubMed - indexed for MEDLINE]Related articles

Intermittent chronic neutropenia in a patient with familial Mediterranean fever.

Ganiou Tidjani K, Ailal F, Najib J, Bellanné-Chantelot C, Donadieu J, Bousfiha AA.

Pediatr Blood Cancer. 2008 Nov;51(5):701-3.PMID: 18661496 [PubMed - indexed for MEDLINE]Related articles

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.

Massin P, Dubois-Laforgue D, Meas T, Laloi-Michelin M, Gin H, Bauduceau B, Bellanné-Chantelot C, Bertin E, Blickle JF, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Dupuy O, Grimaldi A, Guerci B, Kaloustian E, Lecleire-Collet A, Lorenzini F, Murat A, Narbonne H, Olivier F, Paquis-Flucklinger V, Virally M, Vincenot M, Vialettes B, Timsit J, Guillausseau PJ; GEDIAM (Mitochondrial Diabetes French Study Group).

Diabetologia. 2008 Sep;51(9):1664-70. Epub 2008 Jun 26.PMID: 18581092 [PubMed - indexed for MEDLINE]Related articles

New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.

Pierron D, Rocher C, Amati-Bonneau P, Reynier P, Martin-Négrier ML, Allouche S, Batandier C, Mousson de Camaret B, Godinot C, Rotig A, Feldmann D, Bellanne-Chantelot C, Arveiler B, Pennarun E, Rossignol R, Crouzet M, Murail P, Thoraval D, Letellier T.

BMC Med Genet. 2008 May 7;9:41.PMID: 18462486 [PubMed - indexed for MEDLINE]Related articlesFree article

Long-term follow-up of oral glucose tolerance test-derived glucose tolerance and insulin secretion and insulin sensitivity indexes in subjects with glucokinase mutations (MODY2).

Martin D, Bellanné-Chantelot C, Deschamps I, Froguel P, Robert JJ, Velho G.

Diabetes Care. 2008 Jul;31(7):1321-3. Epub 2008 Apr 14.PMID: 18411240 [PubMed - indexed for MEDLINE]Related articlesFree article

[Granulopoeisis and leukemogenesis: lessons from congenital neutropenia]

Donadieu J, Beaupain B, Bellanné-Chantelot C.

Med Sci (Paris). 2008 Mar;24(3):284-9. Review. French. PMID: 18334177 [PubMed - indexed for MEDLINE]Related articles

Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young.

Ellard S, Bellanné-Chantelot C, Hattersley AT; European Molecular Genetics Quality Network (EMQN) MODY group.

Diabetologia. 2008 Apr;51(4):546-53. Epub 2008 Feb 23.PMID: 18297260 [PubMed - indexed for MEDLINE]Related articlesFree article

Massively enlarged polycystic kidneys in monozygotic twins with TCF2/HNF-1beta (hepatocyte nuclear factor-1beta) heterozygous whole-gene deletion.

Faguer S, Bouissou F, Dumazer P, Guitard J, Bellanné-Chantelot C, Chauveau D.

Am J Kidney Dis. 2007 Dec;50(6):1023-7.PMID: 18037103 [PubMed - indexed for MEDLINE]Related articles

The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3.

Bellanné-Chantelot C, Carette C, Riveline JP, Valéro R, Gautier JF, Larger E, Reznik Y, Ducluzeau PH, Sola A, Hartemann-Heurtier A, Lecomte P, Chaillous L, Laloi-Michelin M, Wilhem JM, Cuny P, Duron F, Guerci B, Jeandidier N, Mosnier-Pudar H, Assayag M, Dubois-Laforgue D, Velho G, Timsit J.

Diabetes. 2008 Feb;57(2):503-8. Epub 2007 Nov 14.PMID: 18003757 [PubMed - indexed for MEDLINE]Related articlesFree article

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.

Mefford HC, Clauin S, Sharp AJ, Moller RS, Ullmann R, Kapur R, Pinkel D, Cooper GM, Ventura M, Ropers HH, Tommerup N, Eichler EE, Bellanne-Chantelot C.

Am J Hum Genet. 2007 Nov;81(5):1057-69. Epub 2007 Sep 26.PMID: 17924346 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional imaging of the pancreas: the role of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy.

Ribeiro MJ, Boddaert N, Delzescaux T, Valayannopoulos V, Bellanné-Chantelot C, Jaubert F, Verkarre V, Nihoul-Fékété C, Brunelle F, De Lonlay P.

Endocr Dev. 2007;12:55-66.PMID: 17923769 [PubMed - indexed for MEDLINE]Related articles

Infantile spasms as an epileptic feature of DEND syndrome associated with an activating mutation in the potassium adenosine triphosphate (ATP) channel, Kir6.2.

Bahi-Buisson N, Eisermann M, Nivot S, Bellanné-Chantelot C, Dulac O, Bach N, Plouin P, Chiron C, de Lonlay P.

J Child Neurol. 2007 Sep;22(9):1147-50.PMID: 17890419 [PubMed - indexed for MEDLINE]Related articles

The JAK2(V617F) mutation may be present several years before the occurrence of overt myeloproliferative disorders.

Bellanné-Chantelot C, Jego P, Lionne-Huyghe P, Tulliez M, Najman A; French group on myeloproliferative disorders.

Leukemia. 2008 Feb;22(2):450-1. Epub 2007 Sep 13. No abstract available. PMID: 17851561 [PubMed - indexed for MEDLINE]Related articles

The added value of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 children.

Ribeiro MJ, Boddaert N, Bellanné-Chantelot C, Bourgeois S, Valayannopoulos V, Delzescaux T, Jaubert F, Nihoul-Fékété C, Brunelle F, De Lonlay P.

Eur J Nucl Med Mol Imaging. 2007 Dec;34(12):2120-8. Epub 2007 Jul 28.PMID: 17661030 [PubMed - indexed for MEDLINE]Related articles

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.

Link DC, Kunter G, Kasai Y, Zhao Y, Miner T, McLellan MD, Ries RE, Kapur D, Nagarajan R, Dale DC, Bolyard AA, Boxer LA, Welte K, Zeidler C, Donadieu J, Bellanné-Chantelot C, Vardiman JW, Caligiuri MA, Bloomfield CD, DiPersio JF, Tomasson MH, Graubert TA, Westervelt P, Watson M, Shannon W, Baty J, Mardis ER, Wilson RK, Ley TJ.

Blood. 2007 Sep 1;110(5):1648-55. Epub 2007 May 9.PMID: 17494858 [PubMed - indexed for MEDLINE]Related articlesFree article

Exonic duplication of the hepatocyte nuclear factor-1beta gene (transcription factor 2, hepatic) as a cause of maturity onset diabetes of the young type 5.

Carette C, Vaury C, Barthélémy A, Clauin S, Grünfeld JP, Timsit J, Bellanné-Chantelot C.

J Clin Endocrinol Metab. 2007 Jul;92(7):2844-7. Epub 2007 Apr 17.PMID: 17440011 [PubMed - indexed for MEDLINE]Related articlesFree article

Coexistence in the same family of both focal and diffuse forms of hyperinsulinism.

Valayannopoulos V, Vaxillaire M, Aigrain Y, Jaubert F, Bellanné-Chantelot C, Ribeiro MJ, Brunelle F, Froguel P, Robert JJ, Polak M, Nihoul-Fékété C, de Lonlay P.

Diabetes Care. 2007 Jun;30(6):1590-2. Epub 2007 Mar 23. No abstract available. PMID: 17384337 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma.

Jeannot E, Poussin K, Chiche L, Bacq Y, Sturm N, Scoazec JY, Buffet C, Van Nhieu JT, Bellanné-Chantelot C, de Toma C, Laurent-Puig P, Bioulac-Sage P, Zucman-Rossi J.

Cancer Res. 2007 Mar 15;67(6):2611-6.PMID: 17363580 [PubMed - indexed for MEDLINE]Related articlesFree article

Neonatal cholestatic jaundice as the first symptom of a mutation in the hepatocyte nuclear factor-1beta gene (HNF-1beta).

Beckers D, Bellanné-Chantelot C, Maes M.

J Pediatr. 2007 Mar;150(3):313-4.PMID: 17307554 [PubMed - indexed for MEDLINE]Related articles

Neonatal hyperinsulinism: clinicopathologic correlation.

Delonlay P, Simon A, Galmiche-Rolland L, Giurgea I, Verkarre V, Aigrain Y, Santiago-Ribeiro MJ, Polak M, Robert JJ, Bellanne-Chantelot C, Brunelle F, Nihoul-Fekete C, Jaubert F.

Hum Pathol. 2007 Mar;38(3):387-99. Review.PMID: 17303499 [PubMed - indexed for MEDLINE]Related articles

Two Caucasian families with the hepatocyte nuclear factor-1alpha mutation Tyr218Cys.

Hummel M, Vasseur F, Mathieu C, Bellanne-Chantelot C, Froguel P, Standl E, Füchtenbusch M.

Exp Clin Endocrinol Diabetes. 2007 Jan;115(1):62-4.PMID: 17286239 [PubMed - indexed for MEDLINE]Related articles

Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.

Decramer S, Parant O, Beaufils S, Clauin S, Guillou C, Kessler S, Aziza J, Bandin F, Schanstra JP, Bellanné-Chantelot C.

J Am Soc Nephrol. 2007 Mar;18(3):923-33. Epub 2007 Jan 31.PMID: 17267738 [PubMed - indexed for MEDLINE]Related articlesFree article

Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.

Robins T, Bellanne-Chantelot C, Barbaro M, Cabrol S, Wedell A, Lajic S.

J Mol Med. 2007 Mar;85(3):247-55. Epub 2006 Nov 21.PMID: 17119906 [PubMed - indexed for MEDLINE]Related articles

Molecular mechanisms of neonatal hyperinsulinism.

Giurgea I, Bellanné-Chantelot C, Ribeiro M, Hubert L, Sempoux C, Robert JJ, Blankenstein O, Hussain K, Brunelle F, Nihoul-Fékété C, Rahier J, Jaubert F, de Lonlay P.

Horm Res. 2006;66(6):289-96. Epub 2006 Sep 26. Review.PMID: 17003566 [PubMed - indexed for MEDLINE]Related articles

Genetic and epigenetic defects at the 6q24 imprinted locus in a cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique case with hemizygotic deletion in the critical region.

Diatloff-Zito C, Nicole A, Marcelin G, Labit H, Marquis E, Bellanné-Chantelot C, Robert JJ.

J Med Genet. 2007 Jan;44(1):31-7. Epub 2006 Sep 13.PMID: 16971482 [PubMed - indexed for MEDLINE]Related articles

Cystic kidney disease, chromophobe renal cell carcinoma and TCF2 (HNF1 beta) mutations.

Lebrun G, Vasiliu V, Bellanné-Chantelot C, Bensman A, Ulinski T, Chrétien Y, Grünfeld JP.

Nat Clin Pract Nephrol. 2005 Dec;1(2):115-9.PMID: 16932376 [PubMed - indexed for MEDLINE]Related articles

The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism.

Giurgea I, Sempoux C, Bellanné-Chantelot C, Ribeiro M, Hubert L, Boddaert N, Saudubray JM, Robert JJ, Brunelle F, Rahier J, Jaubert F, Nihoul-Fékété C, de Lonlay P.

J Clin Endocrinol Metab. 2006 Oct;91(10):4118-23. Epub 2006 Aug 1.PMID: 16882742 [PubMed - indexed for MEDLINE]Related articlesFree article

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.

Gloyn AL, Diatloff-Zito C, Edghill EL, Bellanné-Chantelot C, Nivot S, Coutant R, Ellard S, Hattersley AT, Robert JJ.

Eur J Hum Genet. 2006 Jul;14(7):824-30. Epub 2006 May 3.PMID: 16670688 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.

Bellanné-Chantelot C, Chaumarel I, Labopin M, Bellanger F, Barbu V, De Toma C, Delhommeau F, Casadevall N, Vainchenker W, Thomas G, Najman A.

Blood. 2006 Jul 1;108(1):346-52. Epub 2006 Mar 14.PMID: 16537803 [PubMed - indexed for MEDLINE]Related articlesFree article

Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.

de Lonlay P, Simon-Carre A, Ribeiro MJ, Boddaert N, Giurgea I, Laborde K, Bellanné-Chantelot C, Verkarre V, Polak M, Rahier J, Syrota A, Seidenwurm D, Nihoul-Fékété C, Robert JJ, Brunelle F, Jaubert F.

J Clin Endocrinol Metab. 2006 Mar;91(3):933-40. Epub 2006 Jan 10.PMID: 16403819 [PubMed - indexed for MEDLINE]Related articlesFree article

Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.

Ulinski T, Lescure S, Beaufils S, Guigonis V, Decramer S, Morin D, Clauin S, Deschênes G, Bouissou F, Bensman A, Bellanné-Chantelot C.

J Am Soc Nephrol. 2006 Feb;17(2):497-503. Epub 2005 Dec 21.PMID: 16371430 [PubMed - indexed for MEDLINE]Related articlesFree article

Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5.

Bellanné-Chantelot C, Clauin S, Chauveau D, Collin P, Daumont M, Douillard C, Dubois-Laforgue D, Dusselier L, Gautier JF, Jadoul M, Laloi-Michelin M, Jacquesson L, Larger E, Louis J, Nicolino M, Subra JF, Wilhem JM, Young J, Velho G, Timsit J.

Diabetes. 2005 Nov;54(11):3126-32.PMID: 16249435 [PubMed - indexed for MEDLINE]Related articlesFree article

[Congenital hyperinsulinism in newborn and infant]

Giurgea I, Ribeiro MJ, Boddaert N, Touati G, Robert JJ, Saudubray JM, Jaubert F, Bellanné-Chantelot C, Brunelle F, Nihoul-Fékété C, de Lonlay P.

Arch Pediatr. 2005 Nov;12(11):1628-35. Epub 2005 Sep 28. Review. French. PMID: 16198094 [PubMed - indexed for MEDLINE]Related articles

The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay.

Harries LW, Bingham C, Bellanne-Chantelot C, Hattersley AT, Ellard S.

Hum Genet. 2005 Nov;118(2):214-24. Epub 2005 Nov 15.PMID: 16133182 [PubMed - indexed for MEDLINE]Related articles

Congenital hyperinsulinism and mosaic abnormalities of the ploidy.

Giurgea I, Sanlaville D, Fournet JC, Sempoux C, Bellanné-Chantelot C, Touati G, Hubert L, Groos MS, Brunelle F, Rahier J, Henquin JC, Dunne MJ, Jaubert F, Robert JJ, Nihoul-Fékété C, Vekemans M, Junien C, de Lonlay P.

J Med Genet. 2006 Mar;43(3):248-54. Epub 2005 Jul 20.PMID: 16033916 [PubMed - indexed for MEDLINE]Related articlesFree article

Dominantly inherited hyperinsulinaemic hypoglycaemia.

de Lonlay P, Giurgea I, Sempoux C, Touati G, Jaubert F, Rahier J, Ribeiro M, Brunelle F, Nihoul-Fékété C, Robert JJ, Saudubray JM, Stanley C, Bellanné-Chantelot C.

J Inherit Metab Dis. 2005;28(3):267-76. Review.PMID: 15868462 [PubMed - indexed for MEDLINE]Related articles

Germline hepatocyte nuclear factor 1alpha and 1beta mutations in renal cell carcinomas.

Rebouissou S, Vasiliu V, Thomas C, Bellanné-Chantelot C, Bui H, Chrétien Y, Timsit J, Rosty C, Laurent-Puig P, Chauveau D, Zucman-Rossi J.

Hum Mol Genet. 2005 Mar 1;14(5):603-14. Epub 2005 Jan 13.PMID: 15649945 [PubMed - indexed for MEDLINE]Related articlesFree article

Diagnosis and management of maturity-onset diabetes of the young.

Timsit J, Bellanné-Chantelot C, Dubois-Laforgue D, Velho G.

Treat Endocrinol. 2005;4(1):9-18. Review.PMID: 15649097 [PubMed - indexed for MEDLINE]Related articles