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Combined effects of genetic and non‐genetic risk factors affect response to ranibizumab in exudative age‐related macular degeneration

Acta ophthalmologica (Oxford, England), 2015-09, Vol.93 (6), p.e451-e457

2015

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Are CSNK2A1 gene mutations associated with retinal dystrophy? Report of a patient carrier of a novel de novo splice site mutation

Journal of human genetics, 2018-06, Vol.63 (6), p.779-781

2018

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Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism predicts the risk of gastrointestinal toxicity and fatigue induced by irinotecan‐based chemotherapy

Cancer, 2006-03, Vol.106 (5), p.1007-1016

2006

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Case Report: Intestinal Nodular Lymphoid Hyperplasia as First Manifestation of Activated PI3Kδ Syndrome Due to a Novel PIK3CD Variant

Frontiers in pediatrics, 2021-10, Vol.9

2021

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Hepatic expression of endocannabinoid receptors and their novel polymorphisms in primary biliary cirrhosis

Journal of gastroenterology, 2010, Vol.45 (1), p.68-76

2010

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Nerve growth factor: from neurotrophin to neurokine

Trends in neurosciences (Regular ed.), 1996-11, Vol.19 (11), p.514-520

1996

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Metastatic transcriptional pattern revealed by gene expression profiling in primary colorectal carcinoma

International journal of cancer, 2005-06, Vol.115 (2), p.256-262

2005

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Stearoylethanolamide exerts anorexic effects in mice via downregulation of liver stearoyl‐coenzyme A desaturase‐1 mRNA expression

The FASEB journal, 2004-10, Vol.18 (13), p.1580-1582

2004

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Gene expression profile of primary gastric cancer: towards the prediction of lymph node status

Annals of surgical oncology, 2007-03, Vol.14 (3), p.1058-1064

2007

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Cannabidiol, unlike synthetic cannabinoids, triggers activation of RBL-2H3 mast cells

Journal of leukocyte biology, 2007-06, Vol.81 (6), p.1512-1522

2007

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N-(2-Hydroxyethyl)hexadecanamide is orally active in reducing edema formation and inflammatory hyperalgesia by down-modulating mast cell activation

European journal of pharmacology, 1996-04, Vol.300 (3), p.227-236

1996

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Elusive amines: migraine depends on biochemical abnormalities

Neurological sciences, 2022-11, Vol.43 (11), p.6299-6304

2022

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Pathogenesis of Cluster Headache: From Episodic to Chronic Form, the Role of Neurotransmitters and Neuromodulators

Headache, 2019-10, Vol.59 (9), p.1665-1670

2019

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Quercetin Protects Cutaneous Tissue-Associated Cell Types Including Sensory Neurons From Oxidative Stress Induced By Glutathione Depletion: Cooperative Effects of Ascorbic Acid

Free radical biology & medicine, 1997, Vol.22 (4), p.669-678

1997

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Amniotic fluid stem cells improve survival and enhance repair of damaged intestine in necrotising enterocolitis via a COX-2 dependent mechanism

Gut, 2014-02, Vol.63 (2), p.300-309

2014

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A novel CACNA1A R2201W variant in a woman with hemiplegic migraine

Neurological sciences, 2023-09, Vol.44 (9), p.3299-3302

2023

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Pathogenesis of Migraine: Role of Neuromodulators

Headache, 2012-07, Vol.52 (7), p.1155-1163

2012

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Disseminated Mycobacterial Infection With Reactive Polyarthritis (Poncet's Disease) During Immune-suppressive Treatment Including Ustekinumab for Pediatric Crohn's Disease

The Pediatric infectious disease journal, 2024-06, Vol.43 (6), p.543-549

2024

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Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication

Journal of neurology, 2024-04, Vol.271 (4), p.1921-1936

2024

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Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders

Mitochondrion, 2021-11, Vol.61, p.159-164

2021

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Multiple melanomas in ichthyosis with confetti: One more piece of evidence

Australasian journal of dermatology, 2023-11, Vol.64 (4), p.576-578

2023

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Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature

Neurogenetics, 2024-07, Vol.25 (3), p.287-291

2024

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Study of arginine metabolism in medication overuse chronic migraine: possible defect in NO synthesis

Neurological sciences, 2022-04, Vol.43 (4), p.2745-2749

2022

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Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature

American journal of medical genetics. Part A, 2024-09, p.e63848

2024

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THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder

Combined effects of genetic and non‐genetic risk factors affect response to ranibizumab in exudative age‐related macular degeneration

Are CSNK2A1 gene mutations associated with retinal dystrophy? Report of a patient carrier of a novel de novo splice site mutation

Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism predicts the risk of gastrointestinal toxicity and fatigue induced by irinotecan‐based chemotherapy

Case Report: Intestinal Nodular Lymphoid Hyperplasia as First Manifestation of Activated PI3Kδ Syndrome Due to a Novel PIK3CD Variant

Hepatic expression of endocannabinoid receptors and their novel polymorphisms in primary biliary cirrhosis

Nerve growth factor: from neurotrophin to neurokine

Metastatic transcriptional pattern revealed by gene expression profiling in primary colorectal carcinoma

Stearoylethanolamide exerts anorexic effects in mice via downregulation of liver stearoyl‐coenzyme A desaturase‐1 mRNA expression

Gene expression profile of primary gastric cancer: towards the prediction of lymph node status

Cannabidiol, unlike synthetic cannabinoids, triggers activation of RBL-2H3 mast cells

N-(2-Hydroxyethyl)hexadecanamide is orally active in reducing edema formation and inflammatory hyperalgesia by down-modulating mast cell activation

Elusive amines: migraine depends on biochemical abnormalities

Pathogenesis of Cluster Headache: From Episodic to Chronic Form, the Role of Neurotransmitters and Neuromodulators

Quercetin Protects Cutaneous Tissue-Associated Cell Types Including Sensory Neurons From Oxidative Stress Induced By Glutathione Depletion: Cooperative Effects of Ascorbic Acid

Amniotic fluid stem cells improve survival and enhance repair of damaged intestine in necrotising enterocolitis via a COX-2 dependent mechanism

A novel CACNA1A R2201W variant in a woman with hemiplegic migraine

Pathogenesis of Migraine: Role of Neuromodulators

Disseminated Mycobacterial Infection With Reactive Polyarthritis (Poncet's Disease) During Immune-suppressive Treatment Including Ustekinumab for Pediatric Crohn's Disease

Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication

Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders

Multiple melanomas in ichthyosis with confetti: One more piece of evidence

Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature

Study of arginine metabolism in medication overuse chronic migraine: possible defect in NO synthesis

Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature

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