Eroukhmanoff, J. et al. 2017 MRI follow-up is unnecessary in patients with macroprolactinomas and long-term normal prolactin levels on dopamine agonist treatment OBJECTIVE: Both antitumor and antisecretory efficacies of dopamine agonists (DA) make them the first-line treatment of macroprolactinomas. However, there is no guideline for MRI follow-up once... Eur. J. Endocrinol. - issue: 3 - volume: 176 - pages: 323-328.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome. Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol Dis - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Matagne, V. et al. 2017 A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of... Neurobiol. Dis. - issue: - volume: 99 - pages: 1-11.
Froudarakis, ME. et al. 2017 Positive pleural cytology is an indicator for visceral pleural invasion in metastatic pleural effusions INTRODUCTION: In case of undiagnosed pleural effusions, it is necessary to conduct thoracentesis with pleural fluid (PF) cytology. Yet, sensitivity of PF cytology is widely variable as a result of... Clin Respir J - issue: - volume: - pages: .
Froudarakis, ME. et al. 2017 Positive pleural cytology is an indicator for visceral pleural invasion in metastatic pleural effusions INTRODUCTION: In case of undiagnosed pleural effusions, it is necessary to conduct thoracentesis with pleural fluid (PF) cytology. Yet, sensitivity of PF cytology is widely variable as a result of... Clin Respir J - issue: - volume: - pages: .
Noury, J. et al. 2017 Rigid spine syndrome associated with sensory-motor axonal neuropathy resembling Charcot-Marie-Tooth disease is characteristic of Bcl-2-associated athanogene-3 gene mutations even without cardiac involvement INTRODUCTION: Bcl-2-associated athanogene-3 (BAG3) mutations have been described in rare cases of rapidly progressive myofibrillar myopathies. Symptoms begin in the first decade with axial involvement... Muscle Nerve - issue: - volume: - pages: .
Noury, J. et al. 2017 Rigid spine syndrome associated with sensory-motor axonal neuropathy resembling Charcot-Marie-Tooth disease is characteristic of Bcl-2-associated athanogene-3 gene mutations even without cardiac involvement INTRODUCTION: Bcl-2-associated athanogene-3 (BAG3) mutations have been described in rare cases of rapidly progressive myofibrillar myopathies. Symptoms begin in the first decade with axial involvement... Muscle Nerve - issue: - volume: - pages: .
Galvani, G. et al. 2017 Conversion of 3-Bromo-2H-coumarins to 3-(Benzofuran-2-yl)-2H-coumarins under Palladium Catalysis: Synthesis and Photophysical Properties Study An intriguing conversion of 3-bromo-2H-coumarins to 3-(benzofuran-2-yl)-2H-coumarins under palladium catalysis is reported. The process involves, from only one single starting material, three... Org. Lett. - issue: 4 - volume: 19 - pages: 910-913.
Galvani, G. et al. 2017 Conversion of 3-Bromo-2H-coumarins to 3-(Benzofuran-2-yl)-2H-coumarins under Palladium Catalysis: Synthesis and Photophysical Properties Study An intriguing conversion of 3-bromo-2H-coumarins to 3-(benzofuran-2-yl)-2H-coumarins under palladium catalysis is reported. The process involves, from only one single starting material, three... Org. Lett. - issue: 4 - volume: 19 - pages: 910-913.
Grimaldi, S. et al. 2017 Global motor unit number index sum score for assessing the loss of lower motor neurons in amyotrophic lateral sclerosis INTRODUCTION: We propose a motor unit number index (MUNIX) global sum score in amyotrophic lateral sclerosis (ALS) to estimate the loss of functional motor units. METHODS: MUNIX was assessed for 18... Muscle Nerve - issue: - volume: - pages: .
Grimaldi, S. et al. 2017 Global motor unit number index sum score for assessing the loss of lower motor neurons in amyotrophic lateral sclerosis INTRODUCTION: We propose a motor unit number index (MUNIX) global sum score in amyotrophic lateral sclerosis (ALS) to estimate the loss of functional motor units. METHODS: MUNIX was assessed for 18... Muscle Nerve - issue: - volume: - pages: .
Gordon, CT. et al. 2017 De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development Bosma arhinia microphthalmia syndrome (BAMS) is an extremely rare and striking condition characterized by complete absence of the nose with or without ocular defects. We report here that missense... Nature Genet. - issue: 2 - volume: 49 - pages: 249-255.
Duclos, Y. et al. 2017 Motor-evoked potential gain is a helpful test for the detection of corticospinal tract dysfunction in amyotrophic lateral sclerosis OBJECTIVE: The detection of upper motor neuron (UMN) dysfunction is necessary for the diagnosis of amyotrophic lateral sclerosis (ALS). However, signs of UMN dysfunction may be difficult to establish.... Clin Neurophysiol - issue: 2 - volume: 128 - pages: 357-364.
Roux, M. et al. 2017 Hoxa1 and Hoxb1 are required for pharyngeal arch artery development Hox transcription factors play critical roles during early vertebrate development. Previous studies have revealed an overlapping function of Hoxa1 and Hoxb1 during specification of the rhombomeres... Mech Dev - issue: - volume: 143 - pages: 1-8.