G P Ramelli

Summary

Affiliation: Oncology Institute of Southern Switzerland
Country: Switzerland

Publications

  1. doi request reprint Age-dependent presentation of tectal plate tumors: preliminary observations
    Gian P Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    J Child Neurol 26:377-80. 2011
  2. doi request reprint [A clinical approach in neuromuscular diseases in childhood]
    Gian Paolo Ramelli
    Servizio Cantonale di Neuropediatria, Ospedale Regionale Bellinzona e Valli, Bellinzona
    Praxis (Bern 1994) 99:785-92. 2010
  3. ncbi request reprint Dystrobrevin isoform expression in patients with neuromuscular disease
    G P Ramelli
    Department of Paediatrics, Ospedale San Giovanni Bellinzona, Bellinzona, Switzerland
    Clin Neuropathol 29:254-61. 2010
  4. doi request reprint [Non epileptic paroxysmal movements disorders in infant]
    G P Ramelli
    Servizio Cantonale di Neuropediatria, Ospedale Regionale Bellinzona e Valli, Bellinzona
    Praxis (Bern 1994) 98:649-54. 2009
  5. doi request reprint Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study
    Gian Paolo Ramelli
    Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Dev Med Child Neurol 50:953-5. 2008
  6. doi request reprint Spontaneous spinal epidural hematomas in children: can we prevent a negative prognosis?--reflections on 2 cases
    Gian Paolo Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Hopitaux Universitaires, Switzerland
    J Child Neurol 23:564-7. 2008
  7. ncbi request reprint Point mutation tRNA(Ser(UCN)) in a child with hearing loss and myoclonus epilepsy
    Gian Paolo Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    J Child Neurol 21:253-5. 2006
  8. ncbi request reprint Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series
    G P Ramelli
    Department of Paediatrics, Ospedale San Giovanni, 6500 Bellinzona, Switzerland
    Swiss Med Wkly 136:189-93. 2006
  9. ncbi request reprint Swiss physicians' practices of long-term mechanical ventilatory support of patients with Duchenne Muscular Dystrophy
    Gian Paolo Ramelli
    Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Swiss Med Wkly 135:599-604. 2005
  10. ncbi request reprint Swelling of the third nerve in a child with transient oculomotor paresis: a possible cause of ophthalmoplegic migraine
    G P Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Neuropediatrics 31:145-7. 2000

Collaborators

  • P Weber
  • J Pavlovic
  • Jean Marc Burgunder
  • J Weis
  • Jürg Hammer
  • M Tolnay
  • M Steinlin
  • Christine M Stauffer
  • Stefan Widmer
  • C A Hänggeli
  • A Capone Mori
  • E Roulet Perez
  • E Boltshauser
  • R Everts
  • J Luetschg
  • D Gubser Mercati
  • J Marcoz
  • E Keller
  • I Pfister
  • T Schmitt-Mechelke
  • M Weissert
  • Rebecca Donadini
  • Boudewijn van der Weg
  • Mario G Bianchetti
  • Sabine Marchand
  • Luigi Caoduro
  • Benno Widmer
  • Augusto Gallino
  • Renzo Ghisla
  • Fausto Taminelli

Detail Information

Publications16

  1. doi request reprint Age-dependent presentation of tectal plate tumors: preliminary observations
    Gian P Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    J Child Neurol 26:377-80. 2011
    ..The difference between groups was statistically significant. Tumor size was similar in the groups. It is therefore concluded that the presentation of tectal plate tumors varies with age...
  2. doi request reprint [A clinical approach in neuromuscular diseases in childhood]
    Gian Paolo Ramelli
    Servizio Cantonale di Neuropediatria, Ospedale Regionale Bellinzona e Valli, Bellinzona
    Praxis (Bern 1994) 99:785-92. 2010
    ..Careful interpretation of the results most often defines diagnosis. The aim of this article is to establish a work-up according to the patient's symptoms and problems in childhood...
  3. ncbi request reprint Dystrobrevin isoform expression in patients with neuromuscular disease
    G P Ramelli
    Department of Paediatrics, Ospedale San Giovanni Bellinzona, Bellinzona, Switzerland
    Clin Neuropathol 29:254-61. 2010
    ..This study evaluated the expression of dystrobrevin in patients with different neuromuscular diseases...
  4. doi request reprint [Non epileptic paroxysmal movements disorders in infant]
    G P Ramelli
    Servizio Cantonale di Neuropediatria, Ospedale Regionale Bellinzona e Valli, Bellinzona
    Praxis (Bern 1994) 98:649-54. 2009
    ..Most of the time, no treatment will be required, and the families will be informed of the good prognosis. These disorders in infants are discussed in the present review...
  5. doi request reprint Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study
    Gian Paolo Ramelli
    Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Dev Med Child Neurol 50:953-5. 2008
    ..2 duplication as well as the wide genetic complexity of ASD. We suggest that genetic evaluation of ASD should include fluorescence in-situ hybridization analysis of the 22q11.2 chromosomal region...
  6. doi request reprint Spontaneous spinal epidural hematomas in children: can we prevent a negative prognosis?--reflections on 2 cases
    Gian Paolo Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Hopitaux Universitaires, Switzerland
    J Child Neurol 23:564-7. 2008
    ..We also report a similar observation in a 13.5-year-old boy who also suffered from acute paraplegia and had only a partial recovery after urgent decompression...
  7. ncbi request reprint Point mutation tRNA(Ser(UCN)) in a child with hearing loss and myoclonus epilepsy
    Gian Paolo Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    J Child Neurol 21:253-5. 2006
    ..Analysis of mitochondrial DNA in patients with hearing loss and myoclonus epilepsy is recommended, even in the absence of laboratory findings. Therapeutically, ubiquinone and antioxidants can be beneficial...
  8. ncbi request reprint Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series
    G P Ramelli
    Department of Paediatrics, Ospedale San Giovanni, 6500 Bellinzona, Switzerland
    Swiss Med Wkly 136:189-93. 2006
    ..Taken together, these cases add to the spectrum of marked discrepancies in clinical, histopathological and molecular genetic findings in BMD...
  9. ncbi request reprint Swiss physicians' practices of long-term mechanical ventilatory support of patients with Duchenne Muscular Dystrophy
    Gian Paolo Ramelli
    Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Swiss Med Wkly 135:599-604. 2005
    ..This is in contrast to the increasing evidence that these interventions can successfully improve quality of life and prolong survival of affected individuals...
  10. ncbi request reprint Swelling of the third nerve in a child with transient oculomotor paresis: a possible cause of ophthalmoplegic migraine
    G P Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Neuropediatrics 31:145-7. 2000
    ..The clinical profile of the patient suggested transient dysfunction in the context of an ophthalmoplegic migraine. A CT scan was normal, but MRI demonstrated a swollen right oculomotor nerve...
  11. ncbi request reprint The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factors
    M Steinlin
    Neuropaediatric Divisions of the Children s Hospitals in Bern, Zurich, Aarau, Neuchatel, Geneva, Basle, Chur, Bellinzona, Lausanne, Lucerne, Sion, St Gallen, Switzerland
    Neuropediatrics 36:90-7. 2005
    ..The outcome correlated significantly with the size of infarction (p = 0.013) and age at stroke (p = 0.027). The overall mortality was 6%. Paediatric stroke is a multiple risk problem, which leads to important long-term sequelae...
  12. ncbi request reprint Anterior spinal artery syndrome in an adolescent with protein S deficiency
    G P Ramelli
    Department of Pediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    J Child Neurol 16:134-5. 2001
    ..We discuss clinical and radiologic findings in an adolescent presenting with anterior spinal artery syndrome. The laboratory results showed a hereditary protein S deficiency...
  13. ncbi request reprint Family history and behavioral abnormalities in girls with recurrent urinary tract infections: a controlled study
    Christine M Stauffer
    Department of Pediatrics, University Hospital, Bern, Switzerland
    J Urol 171:1663-5. 2004
    ..We evaluated the role of family history, infrequent voiding, poor fluid intake, functional stool retention and inadequate anogenital hygiene or toilet habits in girls with recurrent urinary tract infections...
  14. ncbi request reprint Tele-echocardiography in paediatrics
    Stefan Widmer
    Division of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland
    Eur J Pediatr 162:271-5. 2003
    ..In 191 children (98%), the remote echocardiographic diagnosis was correct as confirmed by follow-up face to face consultations. Three cases were diagnosed incorrectly...
  15. ncbi request reprint Rather mild phenotype in a patient with homozygous null mutations in the alpha-sarcoglycan gene
    Gian Paolo Ramelli
    Swiss Med Wkly 136:96-7. 2006
  16. ncbi request reprint Outbreak of coxsackie B5 virus meningitis in a Scout camp
    Gian Paolo Ramelli
    Pediatr Infect Dis J 23:86-7. 2004