PubMed

Acute Vardenafil Administration Improves Bladder Oxygenation in Spontaneously Hypertensive Rats.

Morelli A, Filippi S, Comeglio P, Sarchielli E, Chavalmane AK, Vignozzi L, Fibbi B, Silvestrini E, Sandner P, Gacci M, Carini M, Vannelli GB, Maggi M.

J Sex Med. 2009 Nov 3. [Epub ahead of print]PMID: 19889145 [PubMed - as supplied by publisher]Related articles

Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion.

Faivre L, Collod-Beroud G, Callewaert B, Child A, Loeys BL, Binquet C, Gautier E, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Beroud C, Bonithon-Kopp C, Claustres M, Stheneur C, Bouchot O, Wolf JE, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G.

Am J Med Genet A. 2009 May;149A(5):854-60.PMID: 19353630 [PubMed - indexed for MEDLINE]Related articles

Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.

Faivre L, Masurel-Paulet A, Collod-Béroud G, Callewaert BL, Child AH, Stheneur C, Binquet C, Gautier E, Chevallier B, Huet F, Loeys BL, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Halliday DJ, Béroud C, Bonithon-Kopp C, Claustres M, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G.

Pediatrics. 2009 Jan;123(1):391-8.PMID: 19117906 [PubMed - indexed for MEDLINE]Related articles

Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation.

Faivre L, Collod-Beroud G, Callewaert B, Child A, Binquet C, Gautier E, Loeys BL, Arbustini E, Mayer K, Arslan-Kirchner M, Stheneur C, Kiotsekoglou A, Comeglio P, Marziliano N, Wolf JE, Bouchot O, Khau-Van-Kien P, Beroud C, Claustres M, Bonithon-Kopp C, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Jondeau G, Boileau C.

Eur J Hum Genet. 2009 Apr;17(4):491-501. Epub 2008 Nov 12.PMID: 19002209 [PubMed - indexed for MEDLINE]Related articlesFree article

Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?

Dundar M, Erkilic K, Argun M, Caglayan AO, Comeglio P, Koseoglu E, Matyas G, Child AH.

Genet Couns. 2008;19(3):319-30.PMID: 18990988 [PubMed - indexed for MEDLINE]Related articles

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.

Faivre L, Collod-Beroud G, Child A, Callewaert B, Loeys BL, Binquet C, Gautier E, Arbustini E, Mayer K, Arslan-Kirchner M, Stheneur C, Kiotsekoglou A, Comeglio P, Marziliano N, Halliday D, Beroud C, Bonithon-Kopp C, Claustres M, Plauchu H, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G.

J Med Genet. 2008 Jun;45(6):384-90. Epub 2008 Feb 29.PMID: 18310266 [PubMed - indexed for MEDLINE]Related articles

Marfan syndrome in South Africa: a molecular genetic approach to diagnosis.

Child A, Comeglio P, Arno G, Beighton P.

S Afr Med J. 2007 Sep;97(9):845-7. No abstract available. PMID: 17985054 [PubMed - indexed for MEDLINE]Related articlesFree article

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.

Faivre L, Collod-Beroud G, Loeys BL, Child A, Binquet C, Gautier E, Callewaert B, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Marziliano N, Dietz HC, Halliday D, Beroud C, Bonithon-Kopp C, Claustres M, Muti C, Plauchu H, Robinson PN, Adès LC, Biggin A, Benetts B, Brett M, Holman KJ, De Backer J, Coucke P, Francke U, De Paepe A, Jondeau G, Boileau C.

Am J Hum Genet. 2007 Sep;81(3):454-66. Epub 2007 Jul 25.PMID: 17701892 [PubMed - indexed for MEDLINE]Related articlesFree article

The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutations.

Comeglio P, Johnson P, Arno G, Brice G, Evans A, Aragon-Martin J, da Silva FP, Kiotsekoglou A, Child A.

Hum Mutat. 2007 Sep;28(9):928.PMID: 17657824 [PubMed - indexed for MEDLINE]Related articles

The -174G/C interleukin-6 promoter polymorphism influences the development of macular oedema following uncomplicated phacoemulsification surgery.

Masood I, Negi A, Vernon SA, Comeglio P, Child AH.

Eye (Lond). 2007 Nov;21(11):1412-5. Epub 2006 Oct 6.PMID: 17024220 [PubMed - indexed for MEDLINE]Related articles

Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 gene.

Elçioglu NH, Akalin F, Elçioglu M, Comeglio P, Child AH.

Genet Couns. 2004;15(2):219-25.PMID: 15287423 [PubMed - indexed for MEDLINE]Related articles

Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.

Evans AL, Bell R, Brice G, Comeglio P, Lipede C, Jeffery S, Mortimer P, Sarfarazi M, Child AH.

J Med Genet. 2003 Sep;40(9):697-703. No abstract available. PMID: 12960217 [PubMed - indexed for MEDLINE]Related articlesFree article

Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.

Collod-Béroud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, Béroud C, Boileau C.

Hum Mutat. 2003 Sep;22(3):199-208. Review.PMID: 12938084 [PubMed - indexed for MEDLINE]Related articles

Muscle fibrillin deficiency in Marfan's syndrome myopathy.

Behan WM, Longman C, Petty RK, Comeglio P, Child AH, Boxer M, Foskett P, Harriman DG.

J Neurol Neurosurg Psychiatry. 2003 May;74(5):633-8.PMID: 12700307 [PubMed - indexed for MEDLINE]Related articlesFree article

Gene symbol: FBN1. Disease: Marfan syndrome.

Comeglio P, Evans AL, Brice GW, Anderlid BM, Child AH.

Hum Genet. 2003 Jan;112(1):104. No abstract available. PMID: 12575662 [PubMed - indexed for MEDLINE]Related articles

Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus.

Comeglio P, Evans AL, Brice G, Cooling RJ, Child AH.

Br J Ophthalmol. 2002 Dec;86(12):1359-62.PMID: 12446365 [PubMed - indexed for MEDLINE]Related articlesFree article

Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome.

Comeglio P, Evans AL, Brice GW, Child AH.

Hum Mutat. 2001 Dec;18(6):546-7.PMID: 11748851 [PubMed - indexed for MEDLINE]Related articles

Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome.

Comeglio P, Evans AL, Brice GW, Child AH.

Hum Mutat. 2001 Sep;18(3):251. Corrected and republished in: Hum Mutat. 2001 Dec;18(6):546-7. PMID: 11524736 [PubMed - indexed for MEDLINE]Related articles

Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: genotype-phenotype correlation.

Pepe G, Giusti B, Evangelisti L, Porciani MC, Brunelli T, Giurlani L, Attanasio M, Fattori R, Bagni C, Comeglio P, Abbate R, Gensini GF.

Clin Genet. 2001 Jun;59(6):444-50.PMID: 11453977 [PubMed - indexed for MEDLINE]Related articles

[Thoracic aortic aneurysm. New evidence for fibrillin-1 involvement]

Pepe G, Giusti B, Attanasio M, Evangelisti L, Brunelli T, Comeglio P, Rossi L, Porciani MC, Giurlani L, Conte R, Gensini GF.

Minerva Cardioangiol. 1999 Dec;47(12):548-9. Italian. No abstract available. PMID: 10670197 [PubMed - indexed for MEDLINE]Related articles

[Marfan's syndrome. Clinical and molecular characterization of 51 Italian patients]

Giurlani L, Pepe G, Giusti B, Attanasio M, Comeglio P, Porciani MC, Evangelisti L, Brunelli T, Lucarini L, Abbate R.

Minerva Cardioangiol. 1999 Dec;47(12):544. Italian. No abstract available. PMID: 10670195 [PubMed - indexed for MEDLINE]Related articles

A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagen.

Pepe G, Bertini E, Giusti B, Brunelli T, Comeglio P, Saitta B, Merlini L, Chu ML, Federici G, Abbate R.

Neuromuscul Disord. 1999 Jun;9(4):264-71.PMID: 10399756 [PubMed - indexed for MEDLINE]Related articles

Microheterogeneity in the distribution of the 844ins68 in the cystathionine beta-synthase gene in Italy.

Giusti B, Camacho-Vanegas O, Attanasio M, Comeglio P, Gori AM, Brunelli T, Prisco D, Gensini GF, Abbate R, Pepe G.

Thromb Res. 1999 May 15;94(4):249-54.PMID: 10336241 [PubMed - indexed for MEDLINE]Related articles

A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha1(VI) collagen chain in an italian family affected by bethlem myopathy.

Pepe G, Giusti B, Bertini E, Brunelli T, Saitta B, Comeglio P, Bolognese A, Merlini L, Federici G, Abbate R, Chu ML.

Biochem Biophys Res Commun. 1999 May 19;258(3):802-7.PMID: 10329467 [PubMed - indexed for MEDLINE]Related articles

Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration.

Gori AM, Pepe G, Attanasio M, Falciani M, Abbate R, Prisco D, Fedi S, Giusti B, Brunelli T, Giusti B, Brunelli T, Comeglio P, Gensini GF, Neri Serneri GG.

Thromb Haemost. 1999 Apr;81(4):589-93.PMID: 10235445 [PubMed - indexed for MEDLINE]Related articles

World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker.

Pepe G, Vanegas OC, Rickards O, Giusti B, Comeglio P, Brunelli T, Marcucci R, Prisco D, Gensini GF, Abbate R.

Hum Genet. 1999 Feb;104(2):126-9.PMID: 10190322 [PubMed - indexed for MEDLINE]Related articles

Cytokine gene expression in human LPS- and IFNgamma-stimulated mononuclear cells is inhibited by heparin.

Attanasio M, Gori AM, Giusti B, Pepe G, Comeglio P, Brunelli T, Prisco D, Abbate R, Gensini GF, Neri Serneri GG.

Thromb Haemost. 1998 May;79(5):959-62.PMID: 9609229 [PubMed - indexed for MEDLINE]Related articles

Different distribution of the double mutant "T833C/68 bp insertion" in cystathionine beta-synthase gene in Northern and Southern Italian populations.

Giusti B, Comeglio P, Attanasio M, Gori AM, Brunelli T, Prisco D, Pepe G, Gensini GF, Abbate R.

Thromb Haemost. 1997 Oct;78(4):1293. No abstract available. PMID: 9365000 [PubMed - indexed for MEDLINE]Related articles

A major involvement of the cardiovascular system in patients affected by Marfan syndrome: novel mutations in fibrillin 1 gene.

Pepe G, Giusti B, Attanasio M, Comeglio P, Porciani MC, Giurlani L, Montesi GF, Calamai GC, Vaccari M, Favilli S, Abbate R, Gensini GF.

J Mol Cell Cardiol. 1997 Jul;29(7):1877-84.PMID: 9236141 [PubMed - indexed for MEDLINE]Related articles

Tissue factor and plasminogen activator inhibitor type 2 expression in human stimulated monocytes is inhibited by heparin.

Pepe G, Giusti B, Attanasio M, Gori AM, Comeglio P, Martini F, Gensini G, Abbate R, Neri Serneri GG.

Semin Thromb Hemost. 1997;23(2):135-41.PMID: 9200337 [PubMed - indexed for MEDLINE]Related articles

D-dimer plasma levels during normal pregnancy measured by specific ELISA.

Francalanci I, Comeglio P, Alessandrello Liotta A, Cellai AP, Fedi S, Parretti E, Mecacci F, Mello G, Prisco D, Abbate R.

Int J Clin Lab Res. 1997;27(1):65-7.PMID: 9144030 [PubMed - indexed for MEDLINE]Related articles

Blood clotting activation during normal pregnancy.

Comeglio P, Fedi S, Liotta AA, Cellai AP, Chiarantini E, Prisco D, Mecacci F, Parretti E, Mello G, Abbate R.

Thromb Res. 1996 Nov 1;84(3):199-202.PMID: 8914219 [PubMed - indexed for MEDLINE]Related articles

Identification of a polymorphic CA repeat in the COL6A2 gene on human chromosome 21q22.3.

Comeglio P, Saitta B, Pepe G, Chu ML.

Hum Hered. 1996 Jul-Aug;46(4):239-40.PMID: 8807328 [PubMed - indexed for MEDLINE]Related articles

Clottable to immunological fibrinogen ratio in plasma from control subjects and hyperfibrinogenemic patients.

Prisco D, Zarone N, Liotta AA, Cellai AP, Comeglio P, Fedi S, Francalanci I, Abbate R.

Haemostasis. 1995 Nov-Dec;25(6):257-63.PMID: 8586315 [PubMed - indexed for MEDLINE]Related articles

D-Dimer in intra-uterine growth retardation and gestational hypertension.

Francalanci I, Comeglio P, Liotta AA, Cellai AP, Fedi S, Parretti E, Mello G, Prisco D, Abbate R.

Thromb Res. 1995 Oct 1;80(1):89-92.PMID: 8578542 [PubMed - indexed for MEDLINE]Related articles

Platelet activation and platelet lipid composition in pulmonary cancer.

Prisco D, Paniccia R, Coppo M, Filippini M, Francalanci I, Brunelli T, Comeglio P, Abbate R.

Prostaglandins Leukot Essent Fatty Acids. 1995 Jul;53(1):65-8.PMID: 7675825 [PubMed - indexed for MEDLINE]Related articles

D-dimer concentrations during normal pregnancy, as measured by ELISA.

Francalanci I, Comeglio P, Liotta AA, Cellai AP, Fedi S, Parretti E, Mello G, Prisco D, Abbate R.

Thromb Res. 1995 Jun 1;78(5):399-405.PMID: 7660356 [PubMed - indexed for MEDLINE]Related articles

Defibrotide reduces monocyte PAI-2 and procoagulant activity.

Abbate R, Gori AM, Martini F, Attanasio M, Comeglio P, Giusti B, Zarone N, Francalanci I, Prisco D, Gensini GF.

Semin Thromb Hemost. 1995;21(2):245-50.PMID: 7660147 [PubMed - indexed for MEDLINE]Related articles

No changes in PAI-1 levels after four-month n-3 PUFA ethyl ester supplementation in healthy subjects.

Prisco D, Paniccia R, Filippini M, Francalanci I, Bandinelli B, Comeglio P, Rostagno C, Abbate R, Neri Serneri GG.

Thromb Res. 1994 Nov 1;76(3):237-44.PMID: 7863474 [PubMed - indexed for MEDLINE]Related articles