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Papers authored by Comeglio P

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Acute vardenafil administration improves bladder oxygenation in spontaneously hypertensive rats.

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

The journal of sexual medicine 7(1 Pt 1):107-20, 2010 Jan - Who cited this? | PubMed ID: 19889145 | Fulltext

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.

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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,

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American journal of medical genetics. Part A 149A(5):854-60, 2009 May - Who cited this? | PubMed ID: 19353630 | Fulltext

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

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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,

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European journal of human genetics : EJHG 17(4):491-501, 2009 Apr - Who cited this? | PubMed ID: 19002209 | Fulltext

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.

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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,

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Pediatrics 123(1):391-8, 2009 Jan - Who cited this? | PubMed ID: 19117906 | Fulltext

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

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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,

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Journal of medical genetics 45(6):384-90, 2008 Jun - Who cited this? | PubMed ID: 18310266 | Fulltext

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

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

Genetic counseling (Geneva, Switzerland) 19(3):319-30, 2008 - Who cited this? | PubMed ID: 18990988 | Fulltext

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

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

Eye (London, England) 21(11):1412-5, 2007 Nov - Who cited this? | PubMed ID: 17024220 | Fulltext

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

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

Human mutation 28(9):928, 2007 Sep - Who cited this? | PubMed ID: 17657824 | Fulltext

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.

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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,

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American journal of human genetics 81(3):454-66, 2007 Sep - Who cited this? | PubMed ID: 17701892 | Fulltext

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

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

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 97(9):845-7, 2007 Sep - Who cited this? | PubMed ID: 17985054 | Fulltext

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

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

Genetic counseling (Geneva, Switzerland) 15(2):219-25, 2004 - Who cited this? | PubMed ID: 15287423 | Fulltext

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

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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,

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Human mutation 22(3):199-208, 2003 Sep - Who cited this? | PubMed ID: 12938084 | Fulltext

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

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

Journal of medical genetics 40(9):697-703, 2003 Sep - Who cited this? | PubMed ID: 12960217 | Fulltext

Muscle fibrillin deficiency in Marfan's syndrome myopathy.

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

Journal of neurology, neurosurgery, and psychiatry 74(5):633-8, 2003 May - Who cited this? | PubMed ID: 12700307 | Fulltext

Gene symbol: FBN1. Disease: Marfan syndrome.

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

Human genetics 112(1):104, 2003 Jan - Who cited this? | PubMed ID: 12575662 | Fulltext

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

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

The British journal of ophthalmology 86(12):1359-62, 2002 Dec - Who cited this? | PubMed ID: 12446365 | Fulltext

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

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

Human mutation 18(6):546-7, 2001 Dec - Who cited this? | PubMed ID: 11748851 | Fulltext

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

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

Human mutation 18(3):251, 2001 Sep - Who cited this? | PubMed ID: 11524736 | Fulltext

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

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

Clinical genetics 59(6):444-50, 2001 Jun - Who cited this? | PubMed ID: 11453977 | Fulltext

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

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

Minerva cardioangiologica 47(12):544, 1999 Dec - Who cited this? | PubMed ID: 10670195 | Fulltext

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

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

Minerva cardioangiologica 47(12):548-9, 1999 Dec - Who cited this? | PubMed ID: 10670197 | Fulltext

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.

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

Neuromuscular disorders : NMD 9(4):264-71, 1999 Jun - Who cited this? | PubMed ID: 10399756 | Fulltext

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.

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

Biochemical and biophysical research communications 258(3):802-7, 1999 May 19 - Who cited this? | PubMed ID: 10329467 | Fulltext

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

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

Thrombosis research 94(4):249-54, 1999 May 15 - Who cited this? | PubMed ID: 10336241 | Fulltext

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

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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, and Neri Serneri GG

Thrombosis and haemostasis 81(4):589-93, 1999 Apr - Who cited this? | PubMed ID: 10235445 | Fulltext

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

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

Human genetics 104(2):126-9, 1999 Feb - Who cited this? | PubMed ID: 10190322 | Fulltext

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

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

Thrombosis and haemostasis 79(5):959-62, 1998 May - Who cited this? | PubMed ID: 9609229 | Fulltext

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

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

Thrombosis and haemostasis 78(4):1293, 1997 Oct - Who cited this? | PubMed ID: 9365000 | Fulltext

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

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

Journal of molecular and cellular cardiology 29(7):1877-84, 1997 Jul - Who cited this? | PubMed ID: 9236141 | Fulltext

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

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

International journal of clinical & laboratory research 27(1):65-7, 1997 - Who cited this? | PubMed ID: 9144030 | Fulltext

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

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

Seminars in thrombosis and hemostasis 23(2):135-41, 1997 - Who cited this? | PubMed ID: 9200337 | Fulltext

Blood clotting activation during normal pregnancy.

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

Thrombosis research 84(3):199-202, 1996 Nov 1 - Who cited this? | PubMed ID: 8914219 | Fulltext

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

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

Human heredity 46(4):239-40, 1996 - Who cited this? | PubMed ID: 8807328 | Fulltext

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

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

Thrombosis research 80(1):89-92, 1995 Oct 1 - Who cited this? | PubMed ID: 8578542 | Fulltext

Platelet activation and platelet lipid composition in pulmonary cancer.

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

Prostaglandins, leukotrienes, and essential fatty acids 53(1):65-8, 1995 Jul - Who cited this? | PubMed ID: 7675825 | Fulltext

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

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

Thrombosis research 78(5):399-405, 1995 Jun 1 - Who cited this? | PubMed ID: 7660356 | Fulltext

Defibrotide reduces monocyte PAI-2 and procoagulant activity.

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

Seminars in thrombosis and hemostasis 21(2):245-50, 1995 - Who cited this? | PubMed ID: 7660147 | Fulltext

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

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

Haemostasis 25(6):257-63, 1995 - Who cited this? | PubMed ID: 8586315 | Fulltext

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

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

Thrombosis research 76(3):237-44, 1994 Nov 1 - Who cited this? | PubMed ID: 7863474 | Fulltext

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