Granel B - Search Results

1

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.

Dodé C, Le Dû N, Cuisset L, Letourneur F, Berthelot JM, Vaudour G, Meyrier A, Watts RA, Scott DG, Nicholls A, Granel B, Frances C, Garcier F, Edery P, Boulinguez S, Domergues JP, Delpech M, Grateau G. Dodé C, et al. Among authors: granel b. Am J Hum Genet. 2002 Jun;70(6):1498-506. doi: 10.1086/340786. Epub 2002 Apr 25. Am J Hum Genet. 2002. PMID: 11992256 Free PMC article.

2

[Hereditary intermittant fever].

Grateau G, Granel B, Hentgen V, Dodé C, Cuisset L, Delpech M. Grateau G, et al. Among authors: granel b. Presse Med. 2004 Oct 9;33(17):1195-206. doi: 10.1016/s0755-4982(04)98889-6. Presse Med. 2004. PMID: 15523291 Review. French.

3

CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes.

Granel B, Philip N, Serratrice J, Ene N, Grateau G, Dodé C, Cuisset L, Disdier P, Berbis P, Delpech M, Weiller PJ. Granel B, et al. Dermatology. 2003;206(3):257-9. doi: 10.1159/000068883. Dermatology. 2003. PMID: 12673085

4

Overlap syndrome between FMF and TRAPS in a patient carrying MEFV and TNFRSF1A mutations.

Granel B, Serratrice J, Dodé C, Grateau G, Disdier P, Weiller PJ. Granel B, et al. Clin Exp Rheumatol. 2007 Jul-Aug;25(4 Suppl 45):S93-5. Clin Exp Rheumatol. 2007. PMID: 17949559

5

[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)].

Hentgen V, Granel B, Dodé C, Cuisset L, Delpech M, Grateau G. Hentgen V, et al. Among authors: granel b. Rev Med Interne. 2003 Dec;24(12):781-5. doi: 10.1016/s0248-8663(03)00216-9. Rev Med Interne. 2003. PMID: 14656637 Review. French.

6

Lysozyme amyloidosis: report of 4 cases and a review of the literature.

Granel B, Valleix S, Serratrice J, Chérin P, Texeira A, Disdier P, Weiller PJ, Grateau G. Granel B, et al. Medicine (Baltimore). 2006 Jan;85(1):66-73. doi: 10.1097/01.md.0000200467.51816.6d. Medicine (Baltimore). 2006. PMID: 16523055 Free article. Review.

7

A family with gastrointestinal amyloidosis associated with variant lysozyme.

Granel B, Serratrice J, Valleix S, Grateau G, Droz D, Lafon J, Sault MC, Chaudier B, Disdier P, Laugier R, Delpech M, Weiller PJ. Granel B, et al. Gastroenterology. 2002 Oct;123(4):1346-9. doi: 10.1053/gast.2002.36022. Gastroenterology. 2002. PMID: 12360495

8

Recurrent hepatic hematoma due to familial lysozyme amyloidosis resolves with conservative management.

Granel B, Valleix S, Le Treut YP, Costello R, Bernard F, Rossi P, Faucher B, Frances Y, Grateau G. Granel B, et al. Amyloid. 2014 Mar;21(1):66-8. doi: 10.3109/13506129.2013.868344. Epub 2014 Jan 16. Amyloid. 2014. PMID: 24433109 No abstract available.

9

A new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.

Jean E, Ebbo M, Valleix S, Benarous L, Heyries L, Grados A, Bernit E, Grateau G, Papo T, Granel B, Daniel L, Harlé JR, Schleinitz N. Jean E, et al. Among authors: granel b. BMC Gastroenterol. 2014 Sep 13;14:159. doi: 10.1186/1471-230X-14-159. BMC Gastroenterol. 2014. PMID: 25217048 Free PMC article.

10

Underdiagnosed amyloidosis: amyloidosis of lysozyme variant.

Granel B, Serratrice J, Disdier P, Weiller PJ, Valleix S, Grateau G, Droz D. Granel B, et al. Am J Med. 2005 Mar;118(3):321-2. doi: 10.1016/j.amjmed.2004.10.022. Am J Med. 2005. PMID: 15745733 No abstract available.

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