Works matching AU Murru, R.

Results: 28

Progressive apraxia of speech in a patient with a C9orf72 mutation.

Published in:

2016

By:

Di Stefano, Francesca;
Melis, Monica;
Cannas, Antonino;
Borghero, Giuseppe;
Murru, Maria R.;
Corongiu, Daniela;
Cuccu, Stefania;
Tranquilli, Stefania;
Marrosu, Maria G.;
Marrosu, Francesco;
Floris, Gianluca

Publication type:

Case Study

Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2016, v. 17, n. 3/4, p. 245, doi. 10.3109/21678421.2015.1111904

By:

Floris, Gianluca;
Borghero, Giuseppe;
Di Stefano, Francesca;
Melis, Rosanna;
Puddu, Roberta;
Fadda, Laura;
Murru, Maria R.;
Corongiu, Daniela;
Cuccu, Stefania;
Tranquilli, Stefania;
Cannas, Antonino;
Marrosu, Maria G.;
Chiò, Adriano;
Marrosu, Francesco

Publication type:

Article

Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015, v. 16, n. 1/2, p. 8, doi. 10.3109/21678421.2014.959450

By:

Floris, Gianluca;
Borghero, Giuseppe;
Cannas, Antonino;
Di Stefano, Francesca;
Ruiu, Elisa;
Murru, Maria R.;
Corongiu, Daniela;
Cuccu, Stefania;
Tranquilli, Stefania;
Sardu, Claudia;
Marrosu, Maria G.;
Chiò, Adriano;
Marrosu, Francesco

Publication type:

Article

MARGINAL ZONE LYMPHOMA INTERNATIONAL PROGNOSTIC INDEX (MZL‐IPI): A PROGNOSTIC SCORE FOR THE ENTIRE SPECTRUM OF MARGINAL ZONE LYMPHOMAS. A FIL AND SPORE‐MER STUDY.

Published in:

Hematological Oncology, 2023, v. 41, p. 102, doi. 10.1002/hon.3163_63

By:

Luminari, S.;
Bommier, C.;
Fabbri, N.;
Nizzoli, M. E.;
Maurer, M. J.;
Tarantino, V.;
Ferrero, S.;
Rattotti, S.;
Merli, M.;
Ferrari, A.;
Murru, R.;
Khurana, A.;
Mwangi, R.;
Deodato, M.;
Del Giudice, I.;
Cencini, E.;
Re, F.;
Visco, C.;
Feldman, A. L.;
Link, B. K.

Publication type:

Article

EFFICACY AND DISCONTINUATION RATE OF IBRUTINIB IN TREATMENT NAIVE CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS WITH TP53 ABNORMALITIES. A REAL‐LIFE CAMPUS CLL STUDY.

Published in:

Hematological Oncology, 2021, v. 39, p. 1, doi. 10.1002/hon.46_2880

By:

Visentin, A.;
Mauro, F. R.;
Cibien, F.;
Vitale, C.;
Reda, G.;
Fresa, A.;
Ciolli, S.;
Pietrasanta, D.;
Marchetti, M.;
Murru, R.;
Gentile, M.;
Rigolin, G. M.;
Quaglia, F. M.;
Scarfò, L.;
Sportoletti, P.;
Pravato, S.;
Romano Gargarella, L.;
Facco, M.;
Piazza, F.;
Coscia, M.

Publication type:

Article

Multiple sclerosis risk: interaction between human leukocyte antigen and the environment in Sardinian population.

Published in:

Multiple Sclerosis (13524585), 2009, v. 15, n. 9, p. 1030, doi. 10.1177/1352458509106745

By:

Cocco, E.;
Sardu, C.;
Murru, R.;
Frau, J.;
Lorefice, L.;
Mamusa, E.;
Contu, P.;
Marrosu, M. G.

Publication type:

Article

Acute Pancreatitis Following Brentuximab Vedotin Therapy for Refractory Hodgkin Lymphoma: A Case Report.

Published in:

Drugs in R&D, 2014, v. 14, n. 1, p. 9, doi. 10.1007/s40268-014-0036-x

By:

Urru, S.;
Mariotti, E.;
Carta, P.;
Massidda, S.;
Marcias, M.;
Murru, R.;
Sanna, P.;
Angelucci, E.

Publication type:

Article

Sensorimotor peripheral neuropathy in an elderly AML patient in complete remission while receiving gemtuzumab ozogamicin as maintenance therapy.

Published in:

2006

By:

Romani, C.;
Murru, R.;
Adamo, F.;
Di Tucci, A.;
Sabiu, D.;
Casula, P.;
Angelucci, E.

Publication type:

Case Study

A case of neurofibromatosis and multiple sclerosis.

Published in:

2010

By:

Spinicci G;
Cherchi MV;
Murru R;
Conti M;
Marrosu MG;
Spinicci, Gabriella;
Cherchi, Maria Valeria;
Murru, Raffaele;
Conti, Maria;
Marrosu, Maria Giovanna

Publication type:

journal article

A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities.

Published in:

Neurological Sciences, 2006, v. 27, n. 1, p. 18, doi. 10.1007/s10072-006-0560-8

By:

Murru, M. R.;
Vannelli, A.;
Marrosu, G.;
Cocco, E.;
Corongiu, D.;
Tranquilli, S.;
Cherchi, M. V.;
Mura, M.;
Barberini, L.;
Mallarini, G.;
Marrosu, M. G.

Publication type:

Article

Association between different morphological types and abnormal karyotypes in early pregnancy loss.

Published in:

Ultrasound in Obstetrics & Gynecology, 2011, v. 37, n. 2, p. 219, doi. 10.1002/uog.7681

By:

Angiolucci, M.;
Murru, R.;
Melis, G.;
Carcassi, C.;
Mais, V.

Publication type:

Article

P09.19: Fetal loss and complications after genetic amniocentesis.

Published in:

Ultrasound in Obstetrics & Gynecology, 2010, v. 36, n. S1, p. 205, doi. 10.1002/uog.8437

By:

Angiolucci, M.;
Murru, R.;
Deidda, S.;
Serra, G.;
Melis, G.;
Carcassi, C.

Publication type:

Article

P09.14: Dilated lateral ventricles and micrognathia by ultrasound examination in fetus with mosaic trisomy 9.

Published in:

Ultrasound in Obstetrics & Gynecology, 2010, v. 36, n. S1, p. 203, doi. 10.1002/uog.8432

By:

Murru, R.;
Angiolucci, M.;
Sammarco, A. M.;
Licheri, V.;
Orrù, S.;
Melis, G.

Publication type:

Article

P15.14: Absence of ultrasound abnormalities in a fetus with a small supernumerary marker chromosome (sSMC) found at prenatal diagnosis.

Published in:

Ultrasound in Obstetrics & Gynecology, 2009, v. 34, n. S1, p. 236, doi. 10.1002/uog.7214

By:

Angiolucci, M.;
Murru, R.;
Mais, V.;
Sammarco, A. M.;
Licheri, V.;
Carcassi, C.;
Melis, G. B.

Publication type:

Article

P16.06: Nuchal translucency and other US markers in cases of trisomy 18.

Published in:

Ultrasound in Obstetrics & Gynecology, 2009, v. 34, n. S1, p. 238, doi. 10.1002/uog.7223

By:

Murru, R.;
Angiolucci, M.;
Deidda, S.;
Serra, G.;
Melis, G. B.;
Orrù, S.

Publication type:

Article

A case of fatal overwhelming microgranular variant (M3v) of acute promyelocytic leukemia with extensive extramedullary involvement.

Published in:

2010

By:

Romani, Claudio;
Murru, R;
Pettinau, M;
Di Tucci, A A;
Culurgioni, F;
Pulisci, D;
Angelucci, E

Publication type:

Case Study

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.

Published in:

Genes & Immunity, 2009, v. 10, n. 1, p. 15, doi. 10.1038/gene.2008.84

By:

Zoledziewska, M.;
Costa, G.;
Pitzalis, M.;
Cocco, E.;
Melis, C.;
Moi, L.;
Zavattari, P.;
Murru, R.;
Lampis, R.;
Morelli, L.;
Poddie, F.;
Frongia, P.;
Pusceddu, P.;
Bajorek, M.;
Marras, A.;
Satta, A M;
Chessa, A.;
Pugliatti, M.;
Sotgiu, S.;
Whalen, M. B.

Publication type:

Article

Long-term seismogenesis in Greece: Comparison of the evolving stress field and precursory scale increase approaches.

Published in:

Journal of Geophysical Research. Solid Earth, 2006, v. 111, n. B5, p. n/a, doi. 10.1029/2005JB003805

By:

Papadimitriou, E. E.;
Evison, F. F.;
Rhoades, D. A.;
Karakostas, V. G.;
Console, R.;
Murru, M. R.

Publication type:

Article

Human breast milk cells are positive for the pioneer transcription factor ISL1.

Published in:

European Review for Medical & Pharmacological Sciences, 2023, v. 27, n. 18, p. 8842

By:

PIRAS, M.;
CONI, P.;
PILUDU, M.;
CONI, S.;
LACHOWICZ, J. I.;
JAREMKO, M.;
FAA, G.;
CAU, F.;
SCANO, A.;
ORRÙ, G.;
MURRU, R.;
PICHIRI, G.

Publication type:

Article

Three is better than two: humoral response in allogeneic HSCT after the third BNT162b2 SARS-CoV-2 mRNA vaccine.

Published in:

2023

By:

BARABINO, L.;
GALITZIA, A.;
MURRU, R.;
CAOCCI, G.;
GRECO, M.;
TARGHETTA, C.;
ANGIONI, G.;
VACCA, A.;
PIRAS, E.;
FRAU, V.;
MULAS, O.;
LA NASA, G.

Publication type:

Letter to the Editor

Clinical course and features of persistent polyclonal B-cell lymphocytosis with BCL-6 amplification during pregnancy.

Published in:

European Review for Medical & Pharmacological Sciences, 2023, v. 27, n. 8, p. 3514

By:

GALITZIA, A.;
MURRU, R.;
CAOCCI, G.;
BARABINO, L.;
AZZENA, A.;
LICHERI, V. M.;
GRECO, M.;
LA NASA, G.

Publication type:

Article

Chronic graft vs. host disease and hypogammaglobulinemia predict a lower immunological response to the BNT162b2 mRNA COVID-19 vaccine after allogeneic hematopoietic stem cell transplantation.

Published in:

European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 23, p. 8984

By:

BARABINO, L.;
GALITZIA, A.;
MURRU, R.;
CAOCCI, G.;
TARGHETTA, C.;
GRECO, M.;
ANGIONI, G.;
MULAS, O.;
VACCA, A.;
PIRAS, E.;
FRAU, V.;
COSTA, A.;
LA NASA, G.

Publication type:

Article

Expression of L1 Cell Adhesion Molecule (L1CAM) in extracellular vesicles in the human spinal cord during development.

Published in:

European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 17, p. 6273

By:

CAU, F.;
FANNI, D.;
MANCHIA, M.;
GEROSA, C.;
PIRAS, M.;
MURRU, R.;
PARIBELLO, P.;
CONGIU, T.;
CONI, P.;
PICHIRI, G.;
PILUDU, M.;
VAN EYKEN, P.;
GIBO, Y.;
LA NASA, G.;
ORRÙ, G.;
SCANO, A.;
COGHE, F.;
SABA, L.;
CASTAGNOLA, M.;
FAA, G.

Publication type:

Article

Interindividual variability in L1CAM expression in the human kidney during development: are there implications for fetal programming of kidney diseases presenting in adulthood?

Published in:

European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 12, p. 4346

By:

CAU, F.;
GEROSA, C.;
MURRU, R.;
PICHIRI, G.;
CONI, P.;
PIRAS, M.;
SCANO, A.;
ORRÙ, G.;
LA NASA, G.;
COGHE, F.;
CASTAGNOLA, M.;
VAN EYKEN, P.;
SABA, L.;
FANNI, D.;
FAA, G.

Publication type:

Article

Acyl-CoA binding protein (ACBP) is highly expressed in the developing human kidney.

Published in:

European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 9, p. 3301

By:

PIRAS, M.;
GEROSA, C.;
FANNI, D.;
CAU, F.;
CONI, P.;
MURRU, R.;
DENOTTI, G.;
ORRÙ, G.;
SCANO, A.;
LEDDA, F.;
VAN EYKEN, P.;
COGHE, F.;
FAA, G.;
CASTAGNOLA, M.

Publication type:

Article

Sinusal bradycardia after receiving intermediate or high dose cytarabine: four cases from a single institution.

Published in:

European Journal of Cancer Care, 2009, v. 18, n. 3, p. 320, doi. 10.1111/j.1365-2354.2008.00953.x

By:

ROMANI, C.;
PETTINAU, M.;
MURRU, R.;
ANGELUCCI, E.

Publication type:

Article

Geographic differences in the incidence of Huntington's disease in Sardinia, Italy.

Published in:

Neurological Sciences, 2021, v. 42, n. 12, p. 5177, doi. 10.1007/s10072-021-05217-y

By:

Muroni, Antonella;
Murru, Maria R.;
Ulgheri, Lucia;
Sechi, Margherita;
Ercoli, Tommaso;
Marrosu, Francesco;
Scaglione, Cesa L.;
Bentivoglio, Anna Rita;
Petracca, Martina;
Soliveri, Paola;
Cocco, Eleonora;
Cuccu, Stefania;
Deriu, Marcello;
Zuccato, Chiara;
Defazio, Giovanni

Publication type:

Article

A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

Published in:

2015

By:

Lorefice, L.;
Tranquilli, S.;
Fenu, G.;
Murru, M.;
Frau, J.;
Rolesu, M.;
Coghe, G.;
Marrosu, F.;
Marrosu, M.;
Cocco, E.;
Murru, M R;
Coghe, G C;
Marrosu, M G

Publication type:

journal article