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Combination Therapy with Nusinersen and Onasemnogene Abeparvovec-xioi in Spinal Muscular Atrophy Type I

Journal of clinical medicine, 2021-11, Vol.10 (23), p.5540

2021

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Further detailed objectification within comparative analysis of quality of life - based on some sociodemographic characteristics/parameters and related statistical analysis - between mothers of children with congenital versus acquired neuropathology

Balneo and PRM Research Journal (Online. English ed.), 2022-09, Vol.13 (3), p.517

2022

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Physical Therapy and Nusinersen Impact on Spinal Muscular Atrophy Rehabilitative Outcome

Frontiers in bioscience (Landmark. Print), 2022-06, Vol.27 (6), p.179-179

2022

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Data regarding physiatric advanced approaches of stabilometric and virtual reality for balance assessment and (re)training in cerebral palsy

Practica medicală (2006), 2020-12, Vol.15 (4), p.390-399

2020

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Changes in pNFH Levels in Cerebrospinal Fluid and Motor Evolution after the Loading Dose with Nusinersen in Different Types of Spinal Muscular Atrophy

Medicina (Kaunas, Lithuania), 2023-07, Vol.59 (7), p.1244

2023

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Clinical and genetic aspects in the Ehlers Danlos syndrome

Revista română de pediatrie, 2020-12, Vol.69 (4), p.354-357

2020

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Innovative therapies in genetic diseases: Cystic fibrosis

Revista română de pediatrie, 2021-03, Vol.70 (1), p.16-20

2021

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Conceptual bases, elements of methodology and narrative aspects resulted from direct clinical experience – afferent to pulmonary rehabilitation in post COVID-19 patients

Revista medicală Română, 2020-12, Vol.67 (4), p.361-366

2020

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1q44 microdeletion syndrome: A new case with potential additional features

Practica medicală (2006), 2021-03, Vol.16 (1), p.92-96

2021

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Clinical and Electrophysiological Changes in Pediatric Spinal Muscular Atrophy after 2 Years of Nusinersen Treatment

Pharmaceutics, 2022-09, Vol.14 (10), p.2074

2022

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Comparative Analysis of the Quality of Life in Families with Children or Adolescents Having Congenital versus Acquired Neuropathology

Children (Basel), 2022-05, Vol.9 (5), p.714

2022

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Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature

Genes, 2022-01, Vol.13 (2), p.212

2022

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Reliability and sources of variability of 3D kinematics and electromyography measurements to assess newly-acquired gait in toddlers with typical development and unilateral cerebral palsy

Journal of electromyography and kinesiology, 2021-06, Vol.58, p.102544-102544, Article 102544

2021

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Findings regarding emotion regulation strategies and quality of life's domains in families having children with spinal muscular atrophy

Journal of medicine and life, 2021-05, Vol.14 (3), p.390-396

2021

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Further detailed objectification within comparative analysis of quality of life - based on some sociodemographic characteris-tics/parameters and related statistical analysis - between mothers of children with congenital versus acquired neuropathology

Balneo and PRM Research Journal (Online. English ed.), 2022-09, Vol.13 (Vol.13, no.3), p.517

2022

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Characteristics of newly acquired gait in toddlers with unilateral cerebral palsy: Implications for early rehabilitation

Annals of physical and rehabilitation medicine, 2021-05, Vol.64 (3), p.101333-101333, Article 101333

2021

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Clinical features and genetics in non-5q spinal muscular atrophy caused by acid ceramidase deficiency

Journal of medicine and life, 2021, Vol.14 (3), p.424-428

2021

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Study on the use of textiles to manufacture mattresses in order to prevent decubitus ulcers due to post-fracture immobilization syndrome in the elderly patient

Industria textilă (Bucharest, Romania : 1994), 2017-01, Vol.68 (4), p.283-288

2017

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Terapii inovative în bolile genetice: Fibroza chistică

Revista română de pediatrie, 2021-03, Vol.70 (1), p.21-25

2021

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Education/Rehabilitation of Balance and Coordination in Children with Cerebral Palsy

Procedia, social and behavioral sciences, 2014-03, Vol.117, p.597-602

2014

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Endometrial stromal sarcoma in a 27-year-old woman. Case report and literature review

Romanian journal of morphology and embryology, 2018, Vol.59 (3), p.933-938

2018

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No. 287 Our Experience With Extracorporeal Shockwave Therapy (ESWT) in Spastic Children With Cerebral Palsy (CP)

PM & R, 2014-08, Vol.6 (8), p.S149-S149

2014

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Plantar support – a perspective of evaluation of children with scoliosis

Biophilia (Fujisawa), 2014, Vol.2014 (2), p.68-68

2014

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Aspecte clinice şi genetice în cadrul sindromului Ehlers Danlos

Revista română de pediatrie, 2020-12, Vol.69 (4), p.358-361

2020

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New VOUS in

Mædica, 2021-03, Vol.16 (1)

2021

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Combination Therapy with Nusinersen and Onasemnogene Abeparvovec-xioi in Spinal Muscular Atrophy Type I

Further detailed objectification within comparative analysis of quality of life - based on some sociodemographic characteristics/parameters and related statistical analysis - between mothers of children with congenital versus acquired neuropathology

Physical Therapy and Nusinersen Impact on Spinal Muscular Atrophy Rehabilitative Outcome

Data regarding physiatric advanced approaches of stabilometric and virtual reality for balance assessment and (re)training in cerebral palsy

Changes in pNFH Levels in Cerebrospinal Fluid and Motor Evolution after the Loading Dose with Nusinersen in Different Types of Spinal Muscular Atrophy

Clinical and genetic aspects in the Ehlers Danlos syndrome

Innovative therapies in genetic diseases: Cystic fibrosis

Conceptual bases, elements of methodology and narrative aspects resulted from direct clinical experience – afferent to pulmonary rehabilitation in post COVID-19 patients

1q44 microdeletion syndrome: A new case with potential additional features

Clinical and Electrophysiological Changes in Pediatric Spinal Muscular Atrophy after 2 Years of Nusinersen Treatment

Comparative Analysis of the Quality of Life in Families with Children or Adolescents Having Congenital versus Acquired Neuropathology

Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature

Reliability and sources of variability of 3D kinematics and electromyography measurements to assess newly-acquired gait in toddlers with typical development and unilateral cerebral palsy

Findings regarding emotion regulation strategies and quality of life's domains in families having children with spinal muscular atrophy

Further detailed objectification within comparative analysis of quality of life - based on some sociodemographic characteris-tics/parameters and related statistical analysis - between mothers of children with congenital versus acquired neuropathology

Characteristics of newly acquired gait in toddlers with unilateral cerebral palsy: Implications for early rehabilitation

Clinical features and genetics in non-5q spinal muscular atrophy caused by acid ceramidase deficiency

Study on the use of textiles to manufacture mattresses in order to prevent decubitus ulcers due to post-fracture immobilization syndrome in the elderly patient

Terapii inovative în bolile genetice: Fibroza chistică

Education/Rehabilitation of Balance and Coordination in Children with Cerebral Palsy

Endometrial stromal sarcoma in a 27-year-old woman. Case report and literature review

No. 287 Our Experience With Extracorporeal Shockwave Therapy (ESWT) in Spastic Children With Cerebral Palsy (CP)

Plantar support – a perspective of evaluation of children with scoliosis

Aspecte clinice şi genetice în cadrul sindromului Ehlers Danlos

New VOUS in

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