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Nonfatal systemic reactions to subcutaneous immunotherapy: a 10-year experience

Journal of investigational allergology & clinical immunology, 1997-05, Vol.7 (3), p.151

1997

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Reggio Emilia (Northern Italy) Interdisciplinary Uveitis Clinic: What We Have Learned in the Last 20 Years

Ocular immunology and inflammation, 2024-10, Vol.32 (8), p.1777-1787

2024

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Prevalence of red ear syndrome in juvenile primary headaches

Cephalalgia, 2011-04, Vol.31 (5), p.597-602

2011

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Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

Journal of medical genetics, 2001-06, Vol.38 (6), p.417-420

2001

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Sentinel lymph node biopsy in head and neck melanoma

Giornale di Chirurgia - Journal of Surgery, 2014-05, Vol.35 (5-6), p.149-155

2014

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Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome

BMC genomics, 2010-07, Vol.3 (1), p.28-28, Article 28

2010

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Analysis of Endothelial Protein C Receptor Gene and Metabolic Profile in Prader‐Willi Syndrome and Obese Subjects

Obesity (Silver Spring, Md.), 2012-09, Vol.20 (9), p.1866-1870

2012

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The role of rhinomanometry after nasal decongestant test in the assessment of adenoid hypertrophy in children

International journal of pediatric otorhinolaryngology, 2012-03, Vol.76 (3), p.352-356

2012

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The role of silicone stents in the treatment of cicatricial tracheal stenoses

The Journal of thoracic and cardiovascular surgery, 2000-12, Vol.120 (6), p.1064-1069

2000

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A new 6-bp SOX-3 polyalanine tract deletion does not segregate with mental retardation

Genetic testing, 2007-06, Vol.11 (2), p.124-127

2007

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Deletions in the mitochondrial DNA and decrease in the oxidative phosphorylation activity of children with fanconi syndrome secondary to antiblastic therapy

American journal of kidney diseases, 1999-07, Vol.34 (1), p.98-106

1999

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Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome

Journal of medical genetics, 1999-03, Vol.36 (3), p.183-186

1999

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Molecular basis of α-thalassemia in Sicily

Human genetics, 1997-03, Vol.99 (3), p.381-386

1997

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The enhancing effect of pyridostigmine on the GH response to GHRH undergoes an accelerated age-related reduction in Down syndrome

Dementia (Basel, Switzerland), 1996-09, Vol.7 (5), p.288-292

1996

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Bilateral non-communicating paraurethral meatus in Prader-Willi syndrome

Gynecological endocrinology, 1997, Vol.11 (2), p.135-137

1997

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Sodium cromoglycate and carbachol-induced bronchoprovocation in asthmatic children

Pediatric pulmonology, 1987-05, Vol.3 (3), p.161-165

1987

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IGF-I levels in prepubertal and pubertal children with Down syndrome

Minerva endocrinologica, 1998-06, Vol.23 (2), p.31

1998

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Fragile X expression in normal and mentally retarded subjects: Effect of treatment with an antifolic agent

American journal of medical genetics, 1988-05, Vol.30 (1-2), p.369-376

1988

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Growth hormone subnormality in down syndrome

American journal of medical genetics, 1992-07, Vol.43 (5), p.894-895

1992

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Fragile X mental retardation: Prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern

American journal of medical genetics, 1986-01, Vol.23 (1-2), p.589-595

1986

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Modification of bronchial hyperreactivity during pollen season in children allergic to grass

Annals of allergy, 1987-02, Vol.58 (2), p.121

1987

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The fragile X in sicily: An epidemiological survey

American journal of medical genetics, 1988-05, Vol.30 (1-2), p.665-672

1988

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Influence of aeroallergens on bronchial reactivity in children sensitized to grass pollens

Annals of allergy, 1986-02, Vol.56 (2), p.138

1986

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Nonfatal systemic reactions to subcutaneous immunotherapy: a 10-year experience

Reggio Emilia (Northern Italy) Interdisciplinary Uveitis Clinic: What We Have Learned in the Last 20 Years

Prevalence of red ear syndrome in juvenile primary headaches

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

Sentinel lymph node biopsy in head and neck melanoma

Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome

Analysis of Endothelial Protein C Receptor Gene and Metabolic Profile in Prader‐Willi Syndrome and Obese Subjects

The role of rhinomanometry after nasal decongestant test in the assessment of adenoid hypertrophy in children

The role of silicone stents in the treatment of cicatricial tracheal stenoses

A new 6-bp SOX-3 polyalanine tract deletion does not segregate with mental retardation

Deletions in the mitochondrial DNA and decrease in the oxidative phosphorylation activity of children with fanconi syndrome secondary to antiblastic therapy

Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome

Molecular basis of α-thalassemia in Sicily

The enhancing effect of pyridostigmine on the GH response to GHRH undergoes an accelerated age-related reduction in Down syndrome

Bilateral non-communicating paraurethral meatus in Prader-Willi syndrome

Sodium cromoglycate and carbachol-induced bronchoprovocation in asthmatic children

IGF-I levels in prepubertal and pubertal children with Down syndrome

Fragile X expression in normal and mentally retarded subjects: Effect of treatment with an antifolic agent

Growth hormone subnormality in down syndrome

Fragile X mental retardation: Prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern

Modification of bronchial hyperreactivity during pollen season in children allergic to grass

The fragile X in sicily: An epidemiological survey

Influence of aeroallergens on bronchial reactivity in children sensitized to grass pollens

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