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L16. The role of glycemic control in the development of preeclampsia in type 1 diabetic women.

Pregnancy hypertension

Mello G, Ottanelli S, Serena C, Tredici Z, Rambaldi MP, Cardini F, Mecacci F.
PMID: 26009047
Pregnancy Hypertens. 2011 Jul-Oct;1(3):248. doi: 10.1016/j.preghy.2011.08.017. Epub 2011 Sep 29.

No abstract available.

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Mello G, Ottanelli S, Serena C, et al. L16. The role of glycemic control in the development of preeclampsia in type 1 diabetic women. Pregnancy Hypertens. 2011;1(3):248doi: 10.1016/j.preghy.2011.08.017.
Mello, G., Ottanelli, S., Serena, C., Tredici, Z., Rambaldi, M. P., Cardini, F., & Mecacci, F. (2011). L16. The role of glycemic control in the development of preeclampsia in type 1 diabetic women. Pregnancy hypertension, 1(3), 248. https://doi.org/10.1016/j.preghy.2011.08.017
Mello, G, et al. "L16. The role of glycemic control in the development of preeclampsia in type 1 diabetic women." Pregnancy hypertension vol. 1,3 (2011): 248. doi: https://doi.org/10.1016/j.preghy.2011.08.017
Mello G, Ottanelli S, Serena C, Tredici Z, Rambaldi MP, Cardini F, Mecacci F. L16. The role of glycemic control in the development of preeclampsia in type 1 diabetic women. Pregnancy Hypertens. 2011 Jul-Oct;1(3):248. doi: 10.1016/j.preghy.2011.08.017. Epub 2011 Sep 29. PMID: 26009047.
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CSNK1A1 mutations and gene expression analysis in myelodysplastic syndromes with del(5q).

British journal of haematology

Bello E, Pellagatti A, Shaw J, Mecucci C, Kušec R, Killick S, Giagounidis A, Raynaud S, Calasanz MJ, Fenaux P, Boultwood J.
PMID: 26085061
Br J Haematol. 2015 Oct;171(2):210-214. doi: 10.1111/bjh.13563. Epub 2015 Jun 18.

Mutations of CSNK1A1, a gene mapping to the commonly deleted region of the 5q- syndrome, have been recently described in patients with del(5q) myelodysplastic syndromes (MDS). Haploinsufficiency of Csnk1a1 in mice has been shown to result in β-catenin activation...

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Bello E, Pellagatti A, Shaw J, et al. CSNK1A1 mutations and gene expression analysis in myelodysplastic syndromes with del(5q). Br J Haematol. 2015;171(2):210-214doi: 10.1111/bjh.13563.
Bello, E., Pellagatti, A., Shaw, J., Mecucci, C., Kušec, R., Killick, S., Giagounidis, A., Raynaud, S., Calasanz, M. J., Fenaux, P., & Boultwood, J. (2015). CSNK1A1 mutations and gene expression analysis in myelodysplastic syndromes with del(5q). British journal of haematology, 171(2), 210-214. https://doi.org/10.1111/bjh.13563
Bello, Erica, et al. "CSNK1A1 mutations and gene expression analysis in myelodysplastic syndromes with del(5q)." British journal of haematology vol. 171,2 (2015): 210-214. doi: https://doi.org/10.1111/bjh.13563
Bello E, Pellagatti A, Shaw J, Mecucci C, Kušec R, Killick S, Giagounidis A, Raynaud S, Calasanz MJ, Fenaux P, Boultwood J. CSNK1A1 mutations and gene expression analysis in myelodysplastic syndromes with del(5q). Br J Haematol. 2015 Oct;171(2):210-214. doi: 10.1111/bjh.13563. Epub 2015 Jun 18. PMID: 26085061; PMCID: PMC4744770.
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Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare "Unpredictable" Event.

Child neurology open

Becocci A, Felice-Civitillo C, Laurent M, Boehlen F, De Luca R, Fluss J.
PMID: 29662916
Child Neurol Open. 2018 Apr 05;5:2329048X18768693. doi: 10.1177/2329048X18768693. eCollection 2018.

Neonatal thrombocytopenia is a rare complication of maternal autoimmune thrombocytopenia, and no maternal predictors of its gravity and potential complications have been identified. Neonatal cerebral hemorrhage, a feared event in the setting of autoimmune thrombocytopenia, is fortunately uncommon, but...

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Becocci A, Felice-Civitillo C, Laurent M, et al. Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare "Unpredictable" Event. Child Neurol Open. 2018;5:2329048X18768693doi: 10.1177/2329048X18768693.
Becocci, A., Felice-Civitillo, C., Laurent, M., Boehlen, F., De Luca, R., & Fluss, J. (2018). Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare "Unpredictable" Event. Child neurology open, 52329048X18768693. https://doi.org/10.1177/2329048X18768693
Becocci, Andrea, et al. "Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare "Unpredictable" Event." Child neurology open vol. 5 (2018): 2329048X18768693. doi: https://doi.org/10.1177/2329048X18768693
Becocci A, Felice-Civitillo C, Laurent M, Boehlen F, De Luca R, Fluss J. Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare "Unpredictable" Event. Child Neurol Open. 2018 Apr 05;5:2329048X18768693. doi: 10.1177/2329048X18768693. eCollection 2018. PMID: 29662916; PMCID: PMC5894894.
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Data-Driven Differential Diagnosis of Dementia Using Multiclass Disease State Index Classifier.

Frontiers in aging neuroscience

Tolonen A, Rhodius-Meester HFM, Bruun M, Koikkalainen J, Barkhof F, Lemstra AW, Koene T, Scheltens P, Teunissen CE, Tong T, Guerrero R, Schuh A, Ledig C, Baroni M, Rueckert D, Soininen H, Remes AM, Waldemar G, Hasselbalch SG, Mecocci P, van der Flier WM, Lötjönen J.
PMID: 29922145
Front Aging Neurosci. 2018 Apr 25;10:111. doi: 10.3389/fnagi.2018.00111. eCollection 2018.

Clinical decision support systems (CDSSs) hold potential for the differential diagnosis of neurodegenerative diseases. We developed a novel CDSS, the PredictND tool, designed for differential diagnosis of different types of dementia. It combines information obtained from multiple diagnostic tests...

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Tolonen A, Rhodius-Meester HFM, Bruun M, et al. Data-Driven Differential Diagnosis of Dementia Using Multiclass Disease State Index Classifier. Front Aging Neurosci. 2018;10:111doi: 10.3389/fnagi.2018.00111.
Tolonen, A., Rhodius-Meester, H. F. M., Bruun, M., Koikkalainen, J., Barkhof, F., Lemstra, A. W., Koene, T., Scheltens, P., Teunissen, C. E., Tong, T., Guerrero, R., Schuh, A., Ledig, C., Baroni, M., Rueckert, D., Soininen, H., Remes, A. M., Waldemar, G., Hasselbalch, S. G., Mecocci, P., van der Flier, W. M., & Lötjönen, J. (2018). Data-Driven Differential Diagnosis of Dementia Using Multiclass Disease State Index Classifier. Frontiers in aging neuroscience, 10111. https://doi.org/10.3389/fnagi.2018.00111
Tolonen, Antti, et al. "Data-Driven Differential Diagnosis of Dementia Using Multiclass Disease State Index Classifier." Frontiers in aging neuroscience vol. 10 (2018): 111. doi: https://doi.org/10.3389/fnagi.2018.00111
Tolonen A, Rhodius-Meester HFM, Bruun M, Koikkalainen J, Barkhof F, Lemstra AW, Koene T, Scheltens P, Teunissen CE, Tong T, Guerrero R, Schuh A, Ledig C, Baroni M, Rueckert D, Soininen H, Remes AM, Waldemar G, Hasselbalch SG, Mecocci P, van der Flier WM, Lötjönen J. Data-Driven Differential Diagnosis of Dementia Using Multiclass Disease State Index Classifier. Front Aging Neurosci. 2018 Apr 25;10:111. doi: 10.3389/fnagi.2018.00111. eCollection 2018. PMID: 29922145; PMCID: PMC5996907.
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Automatic MRI Quantifying Methods in Behavioral-Variant Frontotemporal Dementia Diagnosis.

Dementia and geriatric cognitive disorders extra

Cajanus A, Hall A, Koikkalainen J, Solje E, Tolonen A, Urhemaa T, Liu Y, Haanpää RM, Hartikainen P, Helisalmi S, Korhonen V, Rueckert D, Hasselbalch S, Waldemar G, Mecocci P, Vanninen R, van Gils M, Soininen H, Lötjönen J, Remes AM.
PMID: 29606954
Dement Geriatr Cogn Dis Extra. 2018 Feb 23;8(1):51-59. doi: 10.1159/000486849. eCollection 2018.

AIMS: We assessed the value of automated MRI quantification methods in the differential diagnosis of behavioral-variant frontotemporal dementia (bvFTD) from Alzheimer disease (AD), Lewy body dementia (LBD), and subjective memory complaints (SMC). We also examined the role of the...

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Cajanus A, Hall A, Koikkalainen J, et al. Automatic MRI Quantifying Methods in Behavioral-Variant Frontotemporal Dementia Diagnosis. Dement Geriatr Cogn Dis Extra. 2018;8(1):51-59doi: 10.1159/000486849.
Cajanus, A., Hall, A., Koikkalainen, J., Solje, E., Tolonen, A., Urhemaa, T., Liu, Y., Haanpää, R. M., Hartikainen, P., Helisalmi, S., Korhonen, V., Rueckert, D., Hasselbalch, S., Waldemar, G., Mecocci, P., Vanninen, R., van Gils, M., Soininen, H., Lötjönen, J., & Remes, A. M. (2018). Automatic MRI Quantifying Methods in Behavioral-Variant Frontotemporal Dementia Diagnosis. Dementia and geriatric cognitive disorders extra, 8(1), 51-59. https://doi.org/10.1159/000486849
Cajanus, Antti, et al. "Automatic MRI Quantifying Methods in Behavioral-Variant Frontotemporal Dementia Diagnosis." Dementia and geriatric cognitive disorders extra vol. 8,1 (2018): 51-59. doi: https://doi.org/10.1159/000486849
Cajanus A, Hall A, Koikkalainen J, Solje E, Tolonen A, Urhemaa T, Liu Y, Haanpää RM, Hartikainen P, Helisalmi S, Korhonen V, Rueckert D, Hasselbalch S, Waldemar G, Mecocci P, Vanninen R, van Gils M, Soininen H, Lötjönen J, Remes AM. Automatic MRI Quantifying Methods in Behavioral-Variant Frontotemporal Dementia Diagnosis. Dement Geriatr Cogn Dis Extra. 2018 Feb 23;8(1):51-59. doi: 10.1159/000486849. eCollection 2018. PMID: 29606954; PMCID: PMC5869565.
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ACL Replacement with Synthetic vs. Biological Tendon Grafts: Long-Term Follow-Up Comparison Using Objective Evaluations.

Surgical technology international

Ciapini G, Nulvesu G, Ipponi E, Chiellini F, Mecacci M, Giannini E, Parchi P, Scaglione M.
PMID: 34647314
Surg Technol Int. 2021 Oct 13;39:369-374.

BACKGROUND AND AIM OF THE STUDY: Anterior cruciate ligament (ACL) tears are among the most common articular injuries in sports and can be responsible for knee instability and reduced articular performance. Treatment can be either conservative or operative, and...

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Ciapini G, Nulvesu G, Ipponi E, et al. ACL Replacement with Synthetic vs. Biological Tendon Grafts: Long-Term Follow-Up Comparison Using Objective Evaluations. Surg Technol Int. 2021;39:369-374
Ciapini, G., Nulvesu, G., Ipponi, E., Chiellini, F., Mecacci, M., Giannini, E., Parchi, P., & Scaglione, M. (2021). ACL Replacement with Synthetic vs. Biological Tendon Grafts: Long-Term Follow-Up Comparison Using Objective Evaluations. Surgical technology international, 39369-374.
Ciapini, Gianluca, et al. "ACL Replacement with Synthetic vs. Biological Tendon Grafts: Long-Term Follow-Up Comparison Using Objective Evaluations." Surgical technology international vol. 39 (2021): 369-374.
Ciapini G, Nulvesu G, Ipponi E, Chiellini F, Mecacci M, Giannini E, Parchi P, Scaglione M. ACL Replacement with Synthetic vs. Biological Tendon Grafts: Long-Term Follow-Up Comparison Using Objective Evaluations. Surg Technol Int. 2021 Oct 13;39:369-374. PMID: 34647314.
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Rationale, Design, and Methodology of a Prospective Cohort Study for Coping with Behavioral and Psychological Symptoms of Dementia: The RECage Project.

Journal of Alzheimer's disease : JAD

Poptsi E, Tsolaki M, Bergh S, Cesana BM, Ciceone A, Fabbo A, Frisoni GB, Frölich L, Guazzarini AG, Hugon J, Fascendini S, Lavolpe S, Mecocci P, Peters O, Defanti CA.
PMID: 34366360
J Alzheimers Dis. 2021;82(4):1861-1862. doi: 10.3233/JAD-219008.

No abstract available.

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Poptsi E, Tsolaki M, Bergh S, et al. Rationale, Design, and Methodology of a Prospective Cohort Study for Coping with Behavioral and Psychological Symptoms of Dementia: The RECage Project. J Alzheimers Dis. 2021;82(4):1861-1862doi: 10.3233/JAD-219008.
Poptsi, E., Tsolaki, M., Bergh, S., Cesana, B. M., Ciceone, A., Fabbo, A., Frisoni, G. B., Frölich, L., Guazzarini, A. G., Hugon, J., Fascendini, S., Lavolpe, S., Mecocci, P., Peters, O., & Defanti, C. A. (2021). Rationale, Design, and Methodology of a Prospective Cohort Study for Coping with Behavioral and Psychological Symptoms of Dementia: The RECage Project. Journal of Alzheimer's disease : JAD, 82(4), 1861-1862. https://doi.org/10.3233/JAD-219008
Poptsi, Eleni, et al. "Rationale, Design, and Methodology of a Prospective Cohort Study for Coping with Behavioral and Psychological Symptoms of Dementia: The RECage Project." Journal of Alzheimer's disease : JAD vol. 82,4 (2021): 1861-1862. doi: https://doi.org/10.3233/JAD-219008
Poptsi E, Tsolaki M, Bergh S, Cesana BM, Ciceone A, Fabbo A, Frisoni GB, Frölich L, Guazzarini AG, Hugon J, Fascendini S, Lavolpe S, Mecocci P, Peters O, Defanti CA. Rationale, Design, and Methodology of a Prospective Cohort Study for Coping with Behavioral and Psychological Symptoms of Dementia: The RECage Project. J Alzheimers Dis. 2021;82(4):1861-1862. doi: 10.3233/JAD-219008. PMID: 34366360; PMCID: PMC8485736.
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Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.

Molecular psychiatry

DeMichele-Sweet MAA, Klei L, Creese B, Harwood JC, Weamer EA, McClain L, Sims R, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Alarcón-Martín E, Valero S, Liu Y, Hooli B, Aarsland D, Selbaek G, Bergh S, Rongve A, Saltvedt I, Skjellegrind HK, Engdahl B, Stordal E, Andreassen OA, Djurovic S, Athanasiu L, Seripa D, Borroni B, Albani D, Forloni G, Mecocci P, Serretti A, De Ronchi D, Politis A, Williams J, Mayeux R, Foroud T, Ruiz A, Ballard C, Holmans P, Lopez OL, Kamboh MI, Devlin B, Sweet RA.
PMID: 34112972
Mol Psychiatry. 2021 Oct;26(10):5797-5811. doi: 10.1038/s41380-021-01152-8. Epub 2021 Jun 10.

Psychotic symptoms, defined as the occurrence of delusions or hallucinations, are frequent in Alzheimer disease (AD with psychosis, AD + P). AD + P affects ~50% of individuals with AD, identifies a subgroup with poor outcomes, and is associated...

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DeMichele-Sweet MAA, Klei L, Creese B, et al. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Mol Psychiatry. 2021;26(10):5797-5811doi: 10.1038/s41380-021-01152-8.
DeMichele-Sweet, M. A. A., Klei, L., Creese, B., Harwood, J. C., Weamer, E. A., McClain, L., Sims, R., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Alarcón-Martín, E., Valero, S., Liu, Y., Hooli, B., Aarsland, D., Selbaek, G., Bergh, S., Rongve, A., Saltvedt, I., Skjellegrind, H. K., Engdahl, B., Stordal, E., Andreassen, O. A., Djurovic, S., Athanasiu, L., Seripa, D., Borroni, B., Albani, D., Forloni, G., Mecocci, P., Serretti, A., De Ronchi, D., Politis, A., Williams, J., Mayeux, R., Foroud, T., Ruiz, A., Ballard, C., Holmans, P., Lopez, O. L., Kamboh, M. I., Devlin, B., & Sweet, R. A. (2021). Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Molecular psychiatry, 26(10), 5797-5811. https://doi.org/10.1038/s41380-021-01152-8
DeMichele-Sweet, Mary Ann A, et al. "Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease." Molecular psychiatry vol. 26,10 (2021): 5797-5811. doi: https://doi.org/10.1038/s41380-021-01152-8
DeMichele-Sweet MAA, Klei L, Creese B, Harwood JC, Weamer EA, McClain L, Sims R, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Alarcón-Martín E, Valero S, Liu Y, Hooli B, Aarsland D, Selbaek G, Bergh S, Rongve A, Saltvedt I, Skjellegrind HK, Engdahl B, Stordal E, Andreassen OA, Djurovic S, Athanasiu L, Seripa D, Borroni B, Albani D, Forloni G, Mecocci P, Serretti A, De Ronchi D, Politis A, Williams J, Mayeux R, Foroud T, Ruiz A, Ballard C, Holmans P, Lopez OL, Kamboh MI, Devlin B, Sweet RA. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Mol Psychiatry. 2021 Oct;26(10):5797-5811. doi: 10.1038/s41380-021-01152-8. Epub 2021 Jun 10. PMID: 34112972; PMCID: PMC8660923.
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HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions.

Leukemia

Bruford EA, Antonescu CR, Carroll AJ, Chinnaiyan A, Cree IA, Cross NCP, Dalgleish R, Gale RP, Harrison CJ, Hastings RJ, Huret JL, Johansson B, Le Beau M, Mecucci C, Mertens F, Verhaak R, Mitelman F.
PMID: 34615987
Leukemia. 2021 Nov;35(11):3040-3043. doi: 10.1038/s41375-021-01436-6. Epub 2021 Oct 06.

Gene fusions have been discussed in the scientific literature since they were first detected in cancer cells in the early 1980s. There is currently no standardized way to denote the genes involved in fusions, but in the majority of...

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Bruford EA, Antonescu CR, Carroll AJ, et al. HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia. 2021;35(11):3040-3043doi: 10.1038/s41375-021-01436-6.
Bruford, E. A., Antonescu, C. R., Carroll, A. J., Chinnaiyan, A., Cree, I. A., Cross, N. C. P., Dalgleish, R., Gale, R. P., Harrison, C. J., Hastings, R. J., Huret, J. L., Johansson, B., Le Beau, M., Mecucci, C., Mertens, F., Verhaak, R., & Mitelman, F. (2021). HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia, 35(11), 3040-3043. https://doi.org/10.1038/s41375-021-01436-6
Bruford, Elspeth A, et al. "HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions." Leukemia vol. 35,11 (2021): 3040-3043. doi: https://doi.org/10.1038/s41375-021-01436-6
Bruford EA, Antonescu CR, Carroll AJ, Chinnaiyan A, Cree IA, Cross NCP, Dalgleish R, Gale RP, Harrison CJ, Hastings RJ, Huret JL, Johansson B, Le Beau M, Mecucci C, Mertens F, Verhaak R, Mitelman F. HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia. 2021 Nov;35(11):3040-3043. doi: 10.1038/s41375-021-01436-6. Epub 2021 Oct 06. PMID: 34615987; PMCID: PMC8550944.
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Ultrasound prediction of adverse outcome and perinatal complications at diagnosis of late-onset fetal growth restriction: a cohort study.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology

Dall'Asta A, Stampalija T, Mecacci F, Minopoli M, Schera GBL, Cagninelli G, Ottaviani C, Fantasia I, Barbieri M, Lisi F, Simeone S, Ghi T, Frusca T.
PMID: 34159652
Ultrasound Obstet Gynecol. 2021 Jun 22; doi: 10.1002/uog.23714. Epub 2021 Jun 22.

BACKGROUND: Abnormal umbilical, cerebral and uterine artery Doppler findings and fetal biometry below the 3OBJECTIVE: To evaluate the relationship between the ultrasound parameters measured at diagnosis and perinatal adverse outcome within a cohort of late-onset FGR fetuses.METHODS: This is...

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Dall'Asta A, Stampalija T, Mecacci F, et al. Ultrasound prediction of adverse outcome and perinatal complications at diagnosis of late-onset fetal growth restriction: a cohort study. Ultrasound Obstet Gynecol. 2021;doi: 10.1002/uog.23714.
Dall'Asta, A., Stampalija, T., Mecacci, F., Minopoli, M., Schera, G. B. L., Cagninelli, G., Ottaviani, C., Fantasia, I., Barbieri, M., Lisi, F., Simeone, S., Ghi, T., & Frusca, T. (2021). Ultrasound prediction of adverse outcome and perinatal complications at diagnosis of late-onset fetal growth restriction: a cohort study. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, . https://doi.org/10.1002/uog.23714
Dall'Asta, A, et al. "Ultrasound prediction of adverse outcome and perinatal complications at diagnosis of late-onset fetal growth restriction: a cohort study." Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. (2021). doi: https://doi.org/10.1002/uog.23714
Dall'Asta A, Stampalija T, Mecacci F, Minopoli M, Schera GBL, Cagninelli G, Ottaviani C, Fantasia I, Barbieri M, Lisi F, Simeone S, Ghi T, Frusca T. Ultrasound prediction of adverse outcome and perinatal complications at diagnosis of late-onset fetal growth restriction: a cohort study. Ultrasound Obstet Gynecol. 2021 Jun 22; doi: 10.1002/uog.23714. Epub 2021 Jun 22. PMID: 34159652.
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Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement.

Annals of hematology

Di Giacomo D, Quintini M, Pierini V, Pellanera F, La Starza R, Gorello P, Matteucci C, Crescenzi B, Fiumara PF, Veltroni M, Borlenghi E, Albano F, Forghieri F, Maccaferri M, Bettelli F, Luppi M, Cuneo A, Rossi G, Mecucci C.
PMID: 34859285
Ann Hematol. 2022 Feb;101(2):297-307. doi: 10.1007/s00277-021-04712-8. Epub 2021 Dec 02.

Platelet-derived growth factor receptor B (PDGFRB) gene rearrangements define a unique subgroup of myeloid and lymphoid neoplasms frequently associated with eosinophilia and characterized by high sensitivity to tyrosine kinase inhibition. To date, various PDGFRB/5q32 rearrangements, involving at least 40...

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Di Giacomo D, Quintini M, Pierini V, et al. Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement. Ann Hematol. 2021;101(2):297-307doi: 10.1007/s00277-021-04712-8.
Di Giacomo, D., Quintini, M., Pierini, V., Pellanera, F., La Starza, R., Gorello, P., Matteucci, C., Crescenzi, B., Fiumara, P. F., Veltroni, M., Borlenghi, E., Albano, F., Forghieri, F., Maccaferri, M., Bettelli, F., Luppi, M., Cuneo, A., Rossi, G., & Mecucci, C. (2022). Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement. Annals of hematology, 101(2), 297-307. https://doi.org/10.1007/s00277-021-04712-8
Di Giacomo, Danika, et al. "Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement." Annals of hematology vol. 101,2 (2022): 297-307. doi: https://doi.org/10.1007/s00277-021-04712-8
Di Giacomo D, Quintini M, Pierini V, Pellanera F, La Starza R, Gorello P, Matteucci C, Crescenzi B, Fiumara PF, Veltroni M, Borlenghi E, Albano F, Forghieri F, Maccaferri M, Bettelli F, Luppi M, Cuneo A, Rossi G, Mecucci C. Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement. Ann Hematol. 2022 Feb;101(2):297-307. doi: 10.1007/s00277-021-04712-8. Epub 2021 Dec 02. PMID: 34859285.
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Identification and genetic characterization of a .

Leukemia & lymphoma

Sorel N, Raimbault A, Brizard F, Depaire T, Pierini V, Dupraz C, Millot F, Mecucci C, Chomel JC.
PMID: 34399652
Leuk Lymphoma. 2021 Dec;62(14):3531-3535. doi: 10.1080/10428194.2021.1966784. Epub 2021 Aug 17.

No abstract available.

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Sorel N, Raimbault A, Brizard F, et al. Identification and genetic characterization of a . Leuk Lymphoma. 2021;62(14):3531-3535doi: 10.1080/10428194.2021.1966784.
Sorel, N., Raimbault, A., Brizard, F., Depaire, T., Pierini, V., Dupraz, C., Millot, F., Mecucci, C., & Chomel, J. C. (2021). Identification and genetic characterization of a . Leukemia & lymphoma, 62(14), 3531-3535. https://doi.org/10.1080/10428194.2021.1966784
Sorel, Nathalie, et al. "Identification and genetic characterization of a ." Leukemia & lymphoma vol. 62,14 (2021): 3531-3535. doi: https://doi.org/10.1080/10428194.2021.1966784
Sorel N, Raimbault A, Brizard F, Depaire T, Pierini V, Dupraz C, Millot F, Mecucci C, Chomel JC. Identification and genetic characterization of a . Leuk Lymphoma. 2021 Dec;62(14):3531-3535. doi: 10.1080/10428194.2021.1966784. Epub 2021 Aug 17. PMID: 34399652.
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