Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 53

1.

De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.

Holt RJ, Young RM, Crespo B, Ceroni F, Curry CJ, Bellacchio E, Bax DA, Ciolfi A, Simon M, Fagerberg CR, van Binsbergen E, De Luca A, Memo L, Dobyns WB, Mohammed AA, Clokie SJH, Zazo Seco C, Jiang YH, Sørensen KP, Andersen H, Sullivan J, Powis Z, Chassevent A, Smith-Hicks C, Petrovski S, Antoniadi T, Shashi V, Gelb BD, Wilson SW, Gerrelli D, Tartaglia M, Chassaing N, Calvas P, Ragge NK.

Am J Hum Genet. 2019 Sep 5;105(3):640-657. doi: 10.1016/j.ajhg.2019.07.005. Epub 2019 Aug 8.

2.

A consensus conference report on defining the eligibility criteria for pediatric palliative care in Italy.

Jankovic M, De Zen L, Pellegatta F, Lazzarin P, Bertolotti M, Manfredini L, Aprea A, Memo L, Del Vecchio A, Agostiniani R, Benini F.

Ital J Pediatr. 2019 Jul 22;45(1):89. doi: 10.1186/s13052-019-0681-3.

3.

Is Lactoferrin More Effective in Reducing Late-Onset Sepsis in Preterm Neonates Fed Formula Than in Those Receiving Mother's Own Milk? Secondary Analyses of Two Multicenter Randomized Controlled Trials.

Manzoni P, Militello MA, Rizzollo S, Tavella E, Messina A, Pieretto M, Boano E, Carlino M, Tognato E, Spola R, Perona A, Maule MM, García Sánchez R, Meyer M, Stolfi I, Pugni L, Messner H, Cattani S, Betta PM, Memo L, Decembrino L, Bollani L, Rinaldi M, Fioretti M, Quercia M, Tzialla C, Laforgia N, Mosca F, Magaldi R, Mostert M, Farina D, Tarnow-Mordi W; Italian Task Force for the Study Prevention of Neonatal Fungal Infections; the Italian Society of Neonatology.

Am J Perinatol. 2019 Jul;36(S 02):S120-S125. doi: 10.1055/s-0039-1691807. Epub 2019 Jun 25.

PMID:
31238372
4.

Colorectal cancer screening: The surgery rates they are a-changing. A nationwide study on surgical resections in Italy.

Zorzi M, Gennaro N, Capodaglio G, Urso EDL, Pucciarelli S, Memo L, Carpin E, Corti M, Rugge M, Fedeli U.

Dig Liver Dis. 2019 Feb;51(2):304-309. doi: 10.1016/j.dld.2018.10.011. Epub 2018 Oct 26.

PMID:
30449608
5.

Group B streptococcus late-onset disease,contaminated breast milk and mothers persistently GBS negative: report of 3cases.

Nicolini G, Borellini M, Loizzo V, Creti R, Memo L, Berardi A.

BMC Pediatr. 2018 Jul 5;18(1):214. doi: 10.1186/s12887-018-1192-x.

6.

Media devices in pre-school children: the recommendations of the Italian pediatric society.

Bozzola E, Spina G, Ruggiero M, Memo L, Agostiniani R, Bozzola M, Corsello G, Villani A.

Ital J Pediatr. 2018 Jun 14;44(1):69. doi: 10.1186/s13052-018-0508-7. Review.

7.

Exposure to Gastric Acid Inhibitors Increases the Risk of Infection in Preterm Very Low Birth Weight Infants but Concomitant Administration of Lactoferrin Counteracts This Effect.

Manzoni P, García Sánchez R, Meyer M, Stolfi I, Pugni L, Messner H, Cattani S, Betta PM, Memo L, Decembrino L, Bollani L, Rinaldi M, Fioretti M, Quercia M, Maule M, Tavella E, Mussa A, Tzialla C, Laforgia N, Mosca F, Magaldi R, Mostert M, Farina D; Italian Task Force for the Study, and Prevention of Neonatal Fungal Infections and the Italian Society of Neonatology.

J Pediatr. 2018 Feb;193:62-67.e1. doi: 10.1016/j.jpeds.2017.09.080. Epub 2017 Dec 1.

PMID:
29198543
8.

Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.

Borghesi A, Mencarelli MA, Memo L, Ferrero GB, Bartuli A, Genuardi M, Stronati M, Villani A, Renieri A, Corsello G; their respective Scientific Societies.

Ital J Pediatr. 2017 Nov 3;43(1):100. doi: 10.1186/s13052-017-0418-0. Review.

9.

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Niceta M, Margiotti K, Digilio MC, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici ML, Consoli F, Torrente I, Ruiz-Perez VL, Dallapiccola B, Marino B, De Luca A, Tartaglia M.

Clin Genet. 2018 Mar;93(3):632-639. doi: 10.1111/cge.13128. Epub 2018 Jan 24.

PMID:
28857138
10.

An area-based study on intrapartum antibiotic prophylaxis for preventing group B streptococcus early-onset disease: advances and limitations.

Berardi A, Rossi C, Bacchi Reggiani ML, Bastelli A, Capretti MG, Chiossi C, Fiorini V, Gambini L, Gavioli S, Lanari M, Memo L, Papa I, Pini L, Rizzo MV, Zucchini A, Facchinetti F, Ferrari F.

J Matern Fetal Neonatal Med. 2017 Jul;30(14):1739-1744. doi: 10.1080/14767058.2016.1224832. Epub 2016 Sep 5.

PMID:
27593156
11.

Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants.

Baraldi E, Lanari M, Manzoni P, Rossi GA, Vandini S, Rimini A, Romagnoli C, Colonna P, Biondi A, Biban P, Chiamenti G, Bernardini R, Picca M, Cappa M, Magazzù G, Catassi C, Urbino AF, Memo L, Donzelli G, Minetti C, Paravati F, Di Mauro G, Festini F, Esposito S, Corsello G.

Ital J Pediatr. 2014 Oct 24;40:65. doi: 10.1186/1824-7288-40-65.

12.

Use of erythropoietin is associated with threshold retinopathy of prematurity (ROP) in preterm ELBW neonates: a retrospective, cohort study from two large tertiary NICUs in Italy.

Manzoni P, Memo L, Mostert M, Gallo E, Guardione R, Maestri A, Saia OS, Opramolla A, Calabrese S, Tavella E, Luparia M, Farina D.

Early Hum Dev. 2014 Sep;90 Suppl 2:S29-33. doi: 10.1016/S0378-3782(14)50009-6.

PMID:
25220123
13.

Bovine lactoferrin supplementation for prevention of necrotizing enterocolitis in very-low-birth-weight neonates: a randomized clinical trial.

Manzoni P, Meyer M, Stolfi I, Rinaldi M, Cattani S, Pugni L, Romeo MG, Messner H, Decembrino L, Laforgia N, Vagnarelli F, Memo L, Bordignon L, Maule M, Gallo E, Mostert M, Quercia M, Bollani L, Pedicino R, Renzullo L, Betta P, Ferrari F, Alexander T, Magaldi R, Farina D, Mosca F, Stronati M.

Early Hum Dev. 2014 Mar;90 Suppl 1:S60-5. doi: 10.1016/S0378-3782(14)70020-9.

PMID:
24709463
14.

Human milk feeding prevents retinopathy of prematurity (ROP) in preterm VLBW neonates.

Manzoni P, Stolfi I, Pedicino R, Vagnarelli F, Mosca F, Pugni L, Bollani L, Pozzi M, Gomez K, Tzialla C, Borghesi A, Decembrino L, Mostert M, Latino MA, Priolo C, Galletto P, Gallo E, Rizzollo S, Tavella E, Luparia M, Corona G, Barberi I, Tridapalli E, Faldella G, Vetrano G, Memo L, Saia OS, Bordignon L, Messner H, Cattani S, Della Casa E, Laforgia N, Quercia M, Romeo M, Betta PM, Rinaldi M, Magaldi R, Maule M, Stronati M, Farina D; Italian Task Force for the Study and Prevention of Neonatal Fungal Infections, Italian Society of Neonatology.

Early Hum Dev. 2013 Jun;89 Suppl 1:S64-8. doi: 10.1016/S0378-3782(13)70019-7.

PMID:
23809355
15.

Fetal alcohol spectrum disorders and fetal alcohol syndrome: the state of the art and new diagnostic tools.

Memo L, Gnoato E, Caminiti S, Pichini S, Tarani L.

Early Hum Dev. 2013 Jun;89 Suppl 1:S40-3. doi: 10.1016/S0378-3782(13)70013-6. Review.

PMID:
23809349
16.

Testing ethylglucuronide in maternal hair and nails for the assessment of fetal exposure to alcohol: comparison with meconium testing.

Morini L, Marchei E, Tarani L, Trivelli M, Rapisardi G, Elicio MR, Ramis J, Garcia-Algar O, Memo L, Pacifici R, Groppi A, Danesino P, Pichini S.

Ther Drug Monit. 2013 Jun;35(3):402-7. doi: 10.1097/FTD.0b013e318283f719.

PMID:
23666568
17.

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG.

Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15.

PMID:
23415580
18.

Group B streptococcus late-onset disease: 2003-2010.

Berardi A, Rossi C, Lugli L, Creti R, Bacchi Reggiani ML, Lanari M, Memo L, Pedna MF, Venturelli C, Perrone E, Ciccia M, Tridapalli E, Piepoli M, Contiero R, Ferrari F; GBS Prevention Working Group, Emilia-Romagna.

Pediatrics. 2013 Feb;131(2):e361-8. doi: 10.1542/peds.2012-1231. Epub 2013 Jan 6.

PMID:
23296441
19.

Chromosomal microarray (CMA) analysis in infants with congenital anomalies: when is it really helpful?

Resta N, Memo L.

J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 4:124-6. doi: 10.3109/14767058.2012.715004. Review.

PMID:
22958042
20.

Clinical characteristics and response to prophylactic fluconazole of preterm VLBW neonates with baseline and acquired fungal colonisation in NICU: data from a multicentre RCT.

Manzoni P, Mostert M, Latino MA, Pugni L, Stolfi I, Decembrino L, Vagnarelli F, Corona G, Tridapalli E, Vetrano G, Memo L, Priolo C, Galletto P, Giovannozzi C, Gallo E, Pedicino R, Barberi I, Faldella G, Mosca F, Saia OS, Bollani L, Maragliano R, Ruffinazzi G, Tzialla C, Stronati M, Rizzollo S, Farina D, Benjamin DK Jr, Smith PB, Jacqz-Aigrain E, Kaguelidou F, Cohen-Wolkowiez M; Italian Task Force for the Study and Prevention of Neonatal Fungal Infections; Italian Society of Neonatology.

Early Hum Dev. 2012 May;88 Suppl 2:S60-4. doi: 10.1016/S0378-3782(12)70017-8.

PMID:
22633517
21.

Seizures and EEG patterns in Pallister-Killian syndrome: 13 new Italian patients.

Giordano L, Viri M, Borgatti R, Lodi M, Accorsi P, Faravelli F, Ferretti MC, Grasso R, Memo L, Prola S, Pruna D, Santucci M, Savasta S, Verrotti A, Romeo A.

Eur J Paediatr Neurol. 2012 Nov;16(6):636-41. doi: 10.1016/j.ejpn.2012.03.003. Epub 2012 Mar 29.

PMID:
22464827
22.

Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency.

Salviati L, Trevisson E, Rodriguez Hernandez MA, Casarin A, Pertegato V, Doimo M, Cassina M, Agosto C, Desbats MA, Sartori G, Sacconi S, Memo L, Zuffardi O, Artuch R, Quinzii C, Dimauro S, Hirano M, Santos-Ocaña C, Navas P.

J Med Genet. 2012 Mar;49(3):187-91. doi: 10.1136/jmedgenet-2011-100394.

23.

Bovine lactoferrin prevents invasive fungal infections in very low birth weight infants: a randomized controlled trial.

Manzoni P, Stolfi I, Messner H, Cattani S, Laforgia N, Romeo MG, Bollani L, Rinaldi M, Gallo E, Quercia M, Maule M, Mostert M, Decembrino L, Magaldi R, Mosca F, Vagnarelli F, Memo L, Betta PM, Stronati M, Farina D; Italian Task Force for the Study and Prevention of Neonatal Fungal Infections–the Italian Society of Neonatology.

Pediatrics. 2012 Jan;129(1):116-23. doi: 10.1542/peds.2011-0279. Epub 2011 Dec 19.

PMID:
22184648
24.

Fetal alcohol syndrome: new perspectives for an ancient and underestimated problem.

de Sanctis L, Memo L, Pichini S, Tarani L, Vagnarelli F.

J Matern Fetal Neonatal Med. 2011 Oct;24 Suppl 1:34-7. doi: 10.3109/14767058.2011.607576. Review.

PMID:
21942588
25.

A survey of Italian and Spanish neonatologists and paediatricians regarding awareness of the diagnosis of FAS and FASD and maternal ethanol use during pregnancy.

Vagnarelli F, Palmi I, García-Algar O, Falcon M, Memo L, Tarani L, Spoletini R, Pacifici R, Mortali C, Pierantozzi A, Pichini S.

BMC Pediatr. 2011 Jun 6;11:51. doi: 10.1186/1471-2431-11-51.

26.

Care procedures for healthy term newborn in maternity ward: the "open" nursery.

Memo L, Longo G, Soriani P.

Early Hum Dev. 2011 Mar;87 Suppl 1:S87-8. doi: 10.1016/j.earlhumdev.2011.01.038. Review. No abstract available.

PMID:
21306839
27.

[Gastric adenocarcinoma following "silastic vertical ring gastroplasty": case report].

Belhaj A, Memmo L, Mehdi A, Mboti F, Closset J.

Rev Med Brux. 2010 Sep-Oct;31(5):459-62. Review. French. Erratum in: Rev Med Brux. 2010 Nov-Dec;31(6):556. Memo, L [corrected to Memmo, L].

PMID:
21174648
28.

[The newborn infant with a suspected malformation syndrome].

Memo L.

Minerva Pediatr. 2010 Jun;62(3 Suppl 1):197-8. Review. Italian.

PMID:
21090093
29.

Nicolaides-Baraitser syndrome: two new cases with autism spectrum disorder.

Gana S, Panizzon M, Fongaro D, Selicorni A, Memo L, Scandurra V, Vannucci C, Bigozzi M, Scordo MR.

Clin Dysmorphol. 2011 Jan;20(1):38-41. doi: 10.1097/MCD.0b013e32833edaa9.

PMID:
20802310
30.

Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions.

Bonaglia MC, Marelli S, Novara F, Commodaro S, Borgatti R, Minardo G, Memo L, Mangold E, Beri S, Zucca C, Brambilla D, Molteni M, Giorda R, Weber RG, Zuffardi O.

Eur J Hum Genet. 2010 Dec;18(12):1302-9. doi: 10.1038/ejhg.2010.115. Epub 2010 Jul 21.

31.

Lactoferrin and prevention of late-onset sepsis in the pre-term neonates.

Manzoni P, Decembrino L, Stolfi I, Pugni L, Rinaldi M, Cattani S, Romeo MG, Messner H, Laforgia N, Vagnarelli F, Memo L, Bordignon L, Saia OS, Maule M, Gallo E, Mostert M, Magnani C, Quercia M, Bollani L, Pedicino R, Renzullo L, Betta P, Ferrari F, Magaldi R, Mosca F, Stronati M, Farina D; Italian Task Force for the Study and Prevention of Neonatal Fungal Infections; Italian Society of Neonatology.

Early Hum Dev. 2010 Jul;86 Suppl 1:59-61. doi: 10.1016/j.earlhumdev.2010.01.009. Epub 2010 Feb 6. Review.

PMID:
20138718
32.

[Antalgic therapy in newborn and breast-fed babies].

Memo L, Pieragostini L.

Minerva Pediatr. 2009 Dec;61(6):864-9. Italian. No abstract available.

PMID:
19935577
33.

The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype.

Grasso M, Cecconi M, Boni S, Forzano F, Barbaresi M, Memo L, Perroni L, Faravelli F, Di Maria E.

Mol Cell Probes. 2010 Apr;24(2):107-9. doi: 10.1016/j.mcp.2009.10.006. Epub 2009 Oct 21.

PMID:
19836446
34.

Bovine lactoferrin supplementation for prevention of late-onset sepsis in very low-birth-weight neonates: a randomized trial.

Manzoni P, Rinaldi M, Cattani S, Pugni L, Romeo MG, Messner H, Stolfi I, Decembrino L, Laforgia N, Vagnarelli F, Memo L, Bordignon L, Saia OS, Maule M, Gallo E, Mostert M, Magnani C, Quercia M, Bollani L, Pedicino R, Renzullo L, Betta P, Mosca F, Ferrari F, Magaldi R, Stronati M, Farina D; Italian Task Force for the Study and Prevention of Neonatal Fungal Infections, Italian Society of Neonatology.

JAMA. 2009 Oct 7;302(13):1421-8. doi: 10.1001/jama.2009.1403.

PMID:
19809023
35.

Nursery care of the newborn with malformation syndrome.

Pluchinotta FR, Memo L.

Early Hum Dev. 2009 Oct;85(10 Suppl):S63-5. doi: 10.1016/j.earlhumdev.2009.08.019. Epub 2009 Sep 23.

PMID:
19783387
36.

Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.

Sarkozy A, Carta C, Moretti S, Zampino G, Digilio MC, Pantaleoni F, Scioletti AP, Esposito G, Cordeddu V, Lepri F, Petrangeli V, Dentici ML, Mancini GM, Selicorni A, Rossi C, Mazzanti L, Marino B, Ferrero GB, Silengo MC, Memo L, Stanzial F, Faravelli F, Stuppia L, Puxeddu E, Gelb BD, Dallapiccola B, Tartaglia M.

Hum Mutat. 2009 Apr;30(4):695-702. doi: 10.1002/humu.20955.

37.

The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.

Grugni G, Crinò A, Bosio L, Corrias A, Cuttini M, De Toni T, Di Battista E, Franzese A, Gargantini L, Greggio N, Iughetti L, Livieri C, Naselli A, Pagano C, Pozzan G, Ragusa L, Salvatoni A, Trifirò G, Beccaria L, Bellizzi M, Bellone J, Brunani A, Cappa M, Caselli G, Cerioni V, Delvecchio M, Giardino D, Iannì F, Memo L, Pilotta A, Pomara C, Radetti G, Sacco M, Sanzari A, Sartorio A, Tonini G, Vettor R, Zaglia F, Chiumello G; Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology (ISPED).

Am J Med Genet A. 2008 Apr 1;146A(7):861-72. doi: 10.1002/ajmg.a.32133.

PMID:
18203198
38.

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.

Rossi E, Riegel M, Messa J, Gimelli S, Maraschio P, Ciccone R, Stroppi M, Riva P, Perrotta CS, Mattina T, Memo L, Baumer A, Kucinskas V, Castellan C, Schinzel A, Zuffardi O.

J Med Genet. 2008 Mar;45(3):147-54. Epub 2007 Nov 15.

39.

[Follow-up of the neonate with malformation syndrome].

Memo L, Selicorni A, Zampino G.

Minerva Pediatr. 2007 Oct;59(5):503-6. Italian. No abstract available.

PMID:
17947891
40.

Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.

Zollino M, Lecce R, Murdolo M, Orteschi D, Marangi G, Selicorni A, Midro A, Sorge G, Zampino G, Memo L, Battaglia D, Petersen M, Pandelia E, Gyftodimou Y, Faravelli F, Tenconi R, Garavelli L, Mazzanti L, Fischetto R, Cavalli P, Savasta S, Rodriguez L, Neri G.

Hum Genet. 2007 Dec;122(5):423-30. Epub 2007 Aug 4. Erratum in: Hum Genet. 2008 Apr;123(3):319.

PMID:
17676343
41.

Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation.

Selicorni A, Russo S, Gervasini C, Castronovo P, Milani D, Cavalleri F, Bentivegna A, Masciadri M, Domi A, Divizia MT, Sforzini C, Tarantino E, Memo L, Scarano G, Larizza L.

Clin Genet. 2007 Aug;72(2):98-108.

PMID:
17661813
42.

[Italian guidelines and recommendations for prevention and treatment of pain in the newborn].

Lago P, Ancora G, Bellieni CV, Cavazza A, Cocchi G, Guadagni AM, Memo L, Merazzi D, Pirelli A; Gruppo di Studio II Dolore nel Neonato della Società Italiana di Neonatologia.

Pediatr Med Chir. 2006;28(1-3):24-34. Italian.

PMID:
17533894
43.

Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?

De Gregori M, Pramparo T, Memo L, Gimelli G, Messa J, Rocchi M, Patricelli MG, Ciccone R, Giorda R, Zuffardi O.

Hum Genet. 2005 Nov;118(2):207-13. Epub 2005 Nov 15.

PMID:
16133173
44.

Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth.

Cecconi M, Forzano F, Milani D, Cavani S, Baldo C, Selicorni A, Pantaleoni C, Silengo M, Ferrero GB, Scarano G, Della Monica M, Fischetto R, Grammatico P, Majore S, Zampino G, Memo L, Cordisco EL, Neri G, Pierluigi M, Bricarelli FD, Grasso M, Faravelli F.

Am J Med Genet A. 2005 Apr 30;134(3):247-53.

PMID:
15742365
45.

Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.

Zollino M, Lecce R, Fischetto R, Murdolo M, Faravelli F, Selicorni A, Buttè C, Memo L, Capovilla G, Neri G.

Am J Hum Genet. 2003 Mar;72(3):590-7. Epub 2003 Jan 30.

46.

Two patients with varying combinations of sternal cleft, haemangiomas, midline abdominal raphe, coarctation of the aorta with a right aortic arch.

Crisponi G, Marras AR, Corrias A, Memo L, Gorinati M, Flora PG.

Clin Dysmorphol. 2000 Apr;9(2):103-6.

PMID:
10826620
47.

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.

Tupler R, Bortotto L, Bühler EM, Alkan M, Malik NJ, Bösch-Al Jadooa N, Memo L, Maraschio P.

J Med Genet. 1992 Jan;29(1):53-5.

48.

Inv dup (8) (p21.1----22.1): further case report and a new hypothesis on the origin of the chromosome abnormality.

Gorinati M, Caufin D, Minelli A, Memo L, Gaspardo G, Dodero A.

Clin Genet. 1991 Jan;39(1):55-9.

PMID:
1997216
49.

Cardiac rhabdomyoma as a marker for the prenatal detection of tuberous sclerosis. Case report.

Gava G, Buoso G, Beltrame GL, Memo L, Visentin S, Cavarzerani A.

Br J Obstet Gynaecol. 1990 Dec;97(12):1154-7. No abstract available.

PMID:
2279023
50.

Is C-reactive protein a reliable indicator of bacterial infection in the newborn?

Gussetti N, Ruga E, Giaquinto C, Memo L, Casellato R, D'Elia R.

J Infect Dis. 1989 Nov;160(5):909-10. No abstract available.

PMID:
2809267

Supplemental Content

Support Center