Search Results

Are severity and location of facial trauma risk factors for cervical spine injuries? 10-year analysis based on the use of the AO spine injury classification and the comprehensive facial injury (CFI) score.

• Authors : Canzi G; Maxillofacial Surgery Unit, Department of Neuroscience - Head & Neck, ASST GOM Niguarda, Milan, Italy.; De Ponti E

Subjects: Facial Injuries*/Facial Injuries*/Facial Injuries*/diagnostic imaging ; Facial Injuries*/Facial Injuries*/Facial Injuries*/epidemiology ; Facial Injuries*/Facial Injuries*/Facial Injuries*/complications

• Source: European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society [Eur Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 9301980 Publication Model: Print-Electronic Cited Medium:

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Repercussions of the COVID-19 pandemic on the epidemiology of facial fractures: a retrospective cohort study.

• Authors : de Sousa Lima A; Department of Pathology and Dental Clinic, Health Sciences Center, Federal University of Piauí, Campus Universitário Ministro Petrônio Portella, Teresina, PI, 64049-550, Brazil.; Câmara JVF

• Source: Oral and maxillofacial surgery [Oral Maxillofac Surg] 2023 Dec 07. Date of Electronic Publication: 2023 Dec 07.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101319632 Publication Model: Print-Electronic Cited

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Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.

• Authors : Cardani R; Lab of Muscle Histopathology and Molecular Biology, IRCCS Policlinico San Donato, Milan, Italy.; Giagnacovo M

Subjects: Mutation*; Chloride Channels/Chloride Channels/Chloride Channels/*genetics ; Myotonic Disorders/Myotonic Disorders/Myotonic Disorders/*genetics

• Source: Journal of neurology [J Neurol] 2012 Oct; Vol. 259 (10), pp. 2090-9. Date of Electronic Publication: 2012 Mar 10.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium:

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Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2.

• Authors : Romeo V; Department of Neurosciences, School of Medicine, University of Padova, via Giustiniani, 5, 35128 Padua, Italy. ; Pegoraro E

Subjects: Brain Diseases/Brain Diseases/Brain Diseases/*pathology ; Brain Diseases/Brain Diseases/Brain Diseases/*psychology ; Myotonic Dystrophy/Myotonic Dystrophy/Myotonic Dystrophy/*pathology

• Source: Journal of neurology [J Neurol] 2010 Aug; Vol. 257 (8), pp. 1246-55. Date of Electronic Publication: 2010 Mar 11.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium:

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Erectile dysfunction in myotonic dystrophy type 1 (DM1).

• Authors : Antonini G; Clemenzi A; Bucci E

Subjects: Erectile Dysfunction/Erectile Dysfunction/Erectile Dysfunction/*epidemiology ; Myotonic Dystrophy/Myotonic Dystrophy/Myotonic Dystrophy/*epidemiology; Adolescent

• Source: Journal of neurology [J Neurol] 2009 Apr; Vol. 256 (4), pp. 657-9. Date of Electronic Publication: 2009 Apr 27.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium:

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Association of dopamine D4 receptor (DRD4) exon III repeat polymorphism with temperament in 3-year-old infants.

• Authors : De Luca A; IRCCS-CSS, San Giovanni Rotondo and CSS-Mendel Institute, Rome, Italy.; Rizzardi M

Subjects: Polymorphism, Genetic*; Child Behavior/Child Behavior/Child Behavior/*physiology ; Receptors, Dopamine D2/Receptors, Dopamine D2/Receptors, Dopamine D2/*genetics

• Source: Neurogenetics [Neurogenetics] 2003 Aug; Vol. 4 (4), pp. 207-12. Date of Electronic Publication: 2003 Mar 27.Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print-Electronic Cited

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Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates.

• Authors : De Luca A; Dipartimento di Biopatologia e Diagnostica per Immagini, Sezione di Genetica, Università di Roma Tor Vergata, Via di Tor Vergata 135, 00133 Rome, Italy.; Rizzardi M

Subjects: Adaptation, Psychological* ; Polymorphism, Genetic* ; Temperament*

• Source: Neurogenetics [Neurogenetics] 2001 Mar; Vol. 3 (2), pp. 79-82.Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print Cited Medium:

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A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation.

• Authors : Novelli G; Cattedra di Genetica Umana, Dipartimento di Sanità Pubblica e Biologia Cellulare, Università Tor Vergata di Roma, Italy. ; Semprini S

Subjects: Gene Deletion* ; Genetic Variation* ; Sex Factors*

• Source: Neurogenetics [Neurogenetics] 1997 May; Vol. 1 (1), pp. 29-30.Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print Cited Medium:

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Molecular basis of galactose-1-phosphate uridyltransferase deficiency involving skeletal muscle.

• Authors : Ninfali P; Istituto di Chimica Biologica G. Fornaini, Università di Urbino, Italy.; Bresolin N

Subjects: Muscle, Skeletal/Muscle, Skeletal/Muscle, Skeletal/*enzymology ; UTP-Hexose-1-Phosphate Uridylyltransferase/UTP-Hexose-1-Phosphate Uridylyltransferase/UTP-Hexose-1-Phosphate Uridylyltransferase/*deficiency; Alleles

• Source: Journal of neurology [J Neurol] 1996 Jan; Vol. 243 (1), pp. 102-3.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print Cited Medium: Print

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Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.

• Authors : Massari A; Department of Public Health and Cell Biology, Tor Vergata University, Rome, Italy.; Gennarelli M

Subjects: Repetitive Sequences, Nucleic Acid*; Leukocytes/Leukocytes/Leukocytes/*physiology ; Muscle, Skeletal/Muscle, Skeletal/Muscle, Skeletal/*physiology

• Source: Journal of neurology [J Neurol] 1995 Jun; Vol. 242 (6), pp. 379-83.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print Cited Medium: Print

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