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Year Number of Results
2000 1
2001 2
2002 1
2003 1
2008 1
2009 3
2014 1
2016 1
2017 1
2020 1
2021 2
2022 2
2023 1
2024 0

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15 results

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Page 1
Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis.
Hamada S, Masson E, Chen JM, Sakaguchi R, Rebours V, Buscail L, Matsumoto R, Tanaka Y, Kikuta K, Kataoka F, Sasaki A, Le Rhun M, Audin H, Lachaux A, Caumont B, Lorenzo D, Billiemaz K, Besnard R, Koch S, Lamireau T, De Koninck X; GREPAN (Genetic REsearch on PANcreatitis) Study Group; Génin E, Cooper DN, Mori Y, Masamune A, Férec C. Hamada S, et al. Among authors: billiemaz k. Hum Mutat. 2022 Feb;43(2):228-239. doi: 10.1002/humu.24315. Epub 2021 Dec 28. Hum Mutat. 2022. PMID: 34923708
The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis.
Masson E, Ewers M, Paliwal S, Kume K, Scotet V, Cooper DN, Rebours V, Buscail L, Rouault K; GREPAN (Genetic REsearch on PANcreatitis) Study Group; Abrantes A, Aguilera Munoz L, Albouys J, Alric L, Amiot X, Archambeaud I, Audiau S, Bastide L, Baudon J, Bellaiche G, Bellon S, Bertrand V, Bideau K, Billiemaz K, Billioud C, Bonnefoy S, Borderon C, Bournet B, Breton E, Brugel M, Buscail L, Cadiot G, Camus M, Carpentier-Pourquier M, Chamouard P, Chaput U, Chen JM, Cholet F, Ciocan DM, Clavel C, Coffin B, Coimet-Berger L, Cosconea S, Creveaux I, Culetto A, Daboussi O, De Mestier L, Degand T, D'engremont C, Denis B, Dermine S, Desgrippes, Drouet D'Aubigny A, Enaud R, Fabre A, Férec C, Gargot D, Gelsi E, Gentilcore E, Gincul R, Ginglinger-Favre E, Giovannini M, Gomercic C, Gondran H, Grainville T, Grandval P, Grasset D, Grimaldi S, Grimbert S, Hagege H, Heissat S, Hentic O, Herber-Mayne A, Hervouet M, Hoibian S, Jacques J, Jais B, Kaassis M, Koch S, Lacaze E, Lacroute J, Lamireau T, Laurent L, Le Guillou X, Le Rhun M, Leblanc S, Levy P, Lievre A, Lorenzo D, Maire F, Marcel K, Masson E, Mauillon J, Morgant S, Moussata D, Muller N, Nambot S, Napoleon B, Olivier A, Pagenault M, Pelleti… See abstract for full author list ➔ Masson E, et al. Among authors: billiemaz k. Pancreatology. 2023 Jan;23(1):48-56. doi: 10.1016/j.pan.2022.11.013. Epub 2022 Dec 5. Pancreatology. 2023. PMID: 36517351
Clinical Remission and Psychological Management are Major Issues for the Quality of Life in Pediatric Crohn Disease.
Gourdonneau A, Bruneau L, Ruemmele FM, Norsa L, Takeda A, Le Gall C, Clouzeau H, Rebouissoux L, Dabadie A, Bridoux-Henno L, Rebeuh J, Thomassin N, Viala J, Willot S, Breton A, Coopman S, Spyckerelle C, Languepin J, Bertrand V, Mouterde O, Degas V, Bonneton M, Lemale J, Destombe S, Billiemaz K, Caron N, Borderon C, Dupont C, Triolo V, Jobert A, Lamireau T, Enaud R. Gourdonneau A, et al. Among authors: billiemaz k. J Pediatr Gastroenterol Nutr. 2021 Jan 1;72(1):74-79. doi: 10.1097/MPG.0000000000002865. J Pediatr Gastroenterol Nutr. 2021. PMID: 32740538
[Intestinal volvulus in extremely premature infants].
Billiemaz K, Varlet F, Patural H, Rayet I, Tardieu D, Lavocat MP, Teyssier G. Billiemaz K, et al. Arch Pediatr. 2001 Nov;8(11):1181-4. doi: 10.1016/s0929-693x(01)00632-7. Arch Pediatr. 2001. PMID: 11760668 French.
Loss of α1β1 soluble guanylate cyclase, the major nitric oxide receptor, leads to moyamoya and achalasia.
Hervé D, Philippi A, Belbouab R, Zerah M, Chabrier S, Collardeau-Frachon S, Bergametti F, Essongue A, Berrou E, Krivosic V, Sainte-Rose C, Houdart E, Adam F, Billiemaz K, Lebret M, Roman S, Passemard S, Boulday G, Delaforge A, Guey S, Dray X, Chabriat H, Brouckaert P, Bryckaert M, Tournier-Lasserve E. Hervé D, et al. Among authors: billiemaz k. Am J Hum Genet. 2014 Mar 6;94(3):385-94. doi: 10.1016/j.ajhg.2014.01.018. Epub 2014 Feb 27. Am J Hum Genet. 2014. PMID: 24581742 Free PMC article.
[Prenatal Bartter's syndrome. Report of two cases].
Tourne G, Collet F, Varlet MN, Billiemaz K, Prieur F, Lavocat MP, Seffert P. Tourne G, et al. Among authors: billiemaz k. J Gynecol Obstet Biol Reprod (Paris). 2003 Dec;32(8 Pt 1):751-4. J Gynecol Obstet Biol Reprod (Paris). 2003. PMID: 15067902 French.
15 results