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POMT2 mutation in a patient with 'MEB-like' phenotype. [electronic resource] by
- Mercuri, E
- D'Amico, A
- Tessa, A
- Berardinelli, A
- Pane, M
- Messina, S
- van Reeuwijk, J
- Bertini, E
- Muntoni, F
- Santorelli, F M
Producer: 20061010
In:
Neuromuscular disorders : NMD vol. 16
Availability: No items available.
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15.
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2018 consensus statement by the Spanish Society of Pathology and the Spanish Society of Medical Oncology on the diagnosis and treatment of cancer of unknown primary. [electronic resource] by
- Losa, F
- Iglesias, L
- Pané, M
- Sanz, J
- Nieto, B
- Fusté, V
- de la Cruz-Merino, L
- Concha, Á
- Balañá, C
- Matías-Guiu, X
Producer: 20190128
In:
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico vol. 20
Availability: No items available.
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16.
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A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy letter to the editor of european journal of pediatric neurology regarding the manuscript "single-center experience with intrathecal administration of nusinersen in children with spinal muscular atrophy type 1" written by pechmann and colleagues". [electronic resource] by
- Sansone, V A
- Pane, M
- Messina, S
- Bruno, C
- D'Amico, A
- Albamonte, E
- Catteruccia, M
- Sframeli, M
- Pedemonte, M
- Vita, G
- Bertini, E
- Mercuri, E
Producer: 20180622
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 22
Availability: No items available.
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17.
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Chronic lung disease in very low birth weight infants: Persistence and improvement of a quality improvement process in a tertiary level neonatal intensive care unit. [electronic resource] by
- Birenbaum, H J
- Pfoh, E R
- Helou, S
- Pane, M A
- Marinkovich, G A
- Dentry, A
- Yeh, Hsin-Chieh
- Updegraff, L
- Arnold, C
- Liverman, S
- Cawman, H
Producer: 20170919
In:
Journal of neonatal-perinatal medicine vol. 9
Availability: No items available.
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18.
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Expanding the clinical spectrum of POMT1 phenotype. [electronic resource] by
- D'Amico, A
- Tessa, A
- Bruno, C
- Petrini, S
- Biancheri, R
- Pane, M
- Pedemonte, M
- Ricci, E
- Falace, A
- Rossi, A
- Mercuri, E
- Santorelli, F M
- Bertini, E
Producer: 20060628
In:
Neurology vol. 66
Availability: No items available.
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19.
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The Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): test development and reliability. [electronic resource] by
- Glanzman, A M
- Mazzone, E
- Main, M
- Pelliccioni, M
- Wood, J
- Swoboda, K J
- Scott, C
- Pane, M
- Messina, S
- Bertini, E
- Mercuri, E
- Finkel, R S
Producer: 20100608
In:
Neuromuscular disorders : NMD vol. 20
Availability: No items available.
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20.
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Neurological examination at 6 to 9 months in infants with cystic periventricular leukomalacia. [electronic resource] by
- Ricci, D
- Cowan, F
- Pane, M
- Gallini, F
- Haataja, L
- Luciano, R
- Cesarini, L
- Leone, D
- Donvito, V
- Baranello, G
- Rutherford, M
- Romagnoli, C
- Dubowitz, L
- Mercuri, E
Producer: 20070302
In:
Neuropediatrics vol. 37
Availability: No items available.
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