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M. Saccoliti · SciRah

Researcher profile · Semantic Scholar

M. Saccoliti

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M. Saccoliti — researcher profile on SciRah

h-index: 10
Works: 31
Citations: 487

Most-cited papers

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
J. Schessl, A. Taratuto, C. Sewry, R. Battini +19 more
2009Brain : a journal of neurology100 citations Open access
Semantic Scholar
Tumor cell lines resistant to ALA-mediated photodynamic therapy and possible tools to target surviving cells.
A. Casas, C. Perotti, B. Ortel, G. D. Di Venosa +3 more
2006International Journal of Oncology55 citations Open access
Semantic Scholar
ALA and ALA hexyl ester in free and liposomal formulations for the photosensitisation of tumour organ cultures
A. Casas, C. Perotti, M. Saccoliti, P. Sacca +2 more
2002British Journal of Cancer55 citations Open access
Semantic Scholar
Epithelioid hemangioendothelioma of the central nervous system. Immunohistochemical and ultrastructural observations of a pediatric case.
A. Taratuto, G. Zurbriggen, G. Sevlever, M. Saccoliti
1988Pediatric Neuroscience52 citations
Semantic Scholar
Skeletal Muscle Biopsy Analysis in Reducing Body Myopathy and Other FHL1-Related Disorders
E. Malfatti, M. Olivé, A. Taratuto, P. Richard +21 more
2013Journal of Neuropathology and Experimental Neurology46 citations Open access
Semantic Scholar
Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study.
A. Taratuto, F. Lubieniecki, D. Diaz, M. Schultz +3 more
1999Neuromuscular Disorders37 citations
Semantic Scholar
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studies.
A. Taratuto, H. Akman, M. Saccoliti, M. Riudavets +5 more
2010Neuromuscular Disorders31 citations
Semantic Scholar
Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies
C. Labasse, G. Brochier, A. Taratuto, B. Cadot +26 more
2022Acta Neuropathologica Communications28 citations Open access
Semantic Scholar
HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes
A. Berardo, X. Lornage, M. Johari, T. Evangelista +11 more
2019Journal of Neurology26 citations Open access
Semantic Scholar
Childhood neuronal ceroid-lipofuscinoses in Argentina.
A. L. Taratuto, M. Saccoliti, G. Sevlever, V. Ruggieri +4 more
1995American journal of medical genetics23 citations
Semantic Scholar
Systemic Transplantation of Bone Marrow Mononuclear Cells Promotes Axonal Regeneration and Analgesia in a Model of Wallerian Degeneration
Vanina Usach, M. Malet, Margarita López, L. Lavalle +6 more
2017Transplantation10 citations Open access
Semantic Scholar
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in Argentina.
M. Hawkes, M. Wilken, V. Bruno, Virginia Pujol-Lereis +4 more
2015Arquivos de Neuro-Psiquiatria8 citations Open access
Semantic Scholar
Giant axonal neuropathy (GAN): an immunohistochemical and ultrastructural study report of a Latin American case
A. Taratuto, Gustavo Sevlever, M. Saccoliti, L. Cáceres +1 more
2004Acta Neuropathologica6 citations
Semantic Scholar
Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients
M. Loos, G. Gomez, Lía Mayorga, R. Caraballo +8 more
2021Molecular Genetics and Metabolism Reports5 citations Open access
Semantic Scholar
G.P.1.07 Progressive muscle biopsies morphological changes in long-term follow-up of multiminicore disease related to RYR1 gene
A. Taratuto, M. Saccoliti, Fabiana Lubieniecki, Nicole Monnier +3 more
20093 citations
Semantic Scholar
Non-invasive follicular neoplasm with papillary-like nuclear features: a challenging and infrequent entity in Argentina
M. Sabán, Norma Tolaba, A. Orlandi, S. Deutsch +17 more
2022Endocrine2 citations Open access
Semantic Scholar
G.P.12.06 Progressive muscle biopsies morphological changes in MTM1-related centronuclear congenital myopathy
Fabiana Lubieniecki, V. Biancalana, Norma B. Romero, S. Monges +2 more
20091 citations
Semantic Scholar
Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies
C. Labasse, G. Brochier, A. Taratuto, B. Cadot +26 more
2022Acta Neuropathologica Communications0 citations Open access
Semantic Scholar
GFPT1-related limb-girdle myasthenia: First case reported in Argentina
Marcelo Rugiero, Hernan Gonorazky, Mariela Bettini, M. Saccoliti +5 more
20170 citations
Semantic Scholar
ADULT ONSET HEREDITARY DIFFUSE LEUCOENCEPHALOPATHY WITH AXONAL SPHEROIDS (HDLS): FIRST CASE REPORT IN SOUTH AMERICA (P2.383)
V. Tkachuk, G. Pacio, Ariel Bustos, Marianela Crespo Arizmendi +7 more
2017Neurology0 citations
Semantic Scholar
[Pulmonary tumorlet associated with second neoplasia].
M. Pitzzu, Y. Ferreira, M. C. Sánchez, M. Saccoliti +5 more
2017Medicina0 citations
Semantic Scholar
Limb-girdle muscular dystrophy 1 G (LGMD1G) with numerous rimmed vacuoles due to a defect in the RNA-binding protein HNRNPDL – Report of an Argentinian family of Italian ancestry
X. Lornage, N. B. Romero, Jocelyn Laporte, A. Dubrovsky +3 more
20160 citations
Semantic Scholar
Expanding the clinical and molecular findings in a patient with Pompe disease
Fabiana Lubieniecki, J. Mozzoni, M. de Castro, E. Foncuberta +4 more
20160 citations
Semantic Scholar
G.P.265
S. Monges, Fabiana Lubieniecki, F. Castro, J. Mozzoni +8 more
20140 citations
Semantic Scholar
G.P.120 FHL1-related Reducing Body Myopathy and Emery–Dreifuss muscular dystrophy: A comparative histoenzymological, immunohistochemical and ultrastructural study
E. Malfatti, M. Olivé, A. Taratuto, P. Richard +13 more
20120 citations
Semantic Scholar
P3.36. Phenotypic spectrum in myopathies with tubular aggregates
Fabian Funk, C. C. Groote, J.-J. Martin, A. Meinhardt +8 more
20110 citations
Semantic Scholar
P2.10 A new form of congenital muscular dystrophy with subsarcolemmal inclusions arising from disintegrated myonuclei
A. Taratuto, I. Nelson, M. Olivé, H. Waisburg +7 more
20110 citations
Semantic Scholar
P2.9 LMNA-related congenital muscular dystrophy: Clinical, pathological and molecular findings
M. Monges, Fabiana Lubieniecki, S. Quijano-Roy, M. Saccoliti +3 more
20110 citations
Semantic Scholar
G.P.16.04. Branching enzyme deficiency should be considered in the differential diagnosis of severe congenital hypotonia
A. Taratuto, H. Akman, M. Saccoliti, M. Riudavets +6 more
20080 citations
Semantic Scholar
LAMININ α2 (MEROSIN) DEFICIENCY RELEVANCE FOR ABNORMAL CORTICAL GYRATION
F. Lubieniecki, D. Diaz, M. Schultz, V. Ruggeri +2 more
19990 citations
Semantic Scholar
[Spastic paraplegia and primary adrenal insufficiency: a case of adrenomyeloneuropathy].
A. Sánchez, R. Parma, M. Echecury, N. Vázquez +4 more
1988Medicina0 citations
Semantic Scholar

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A. Taratuto×13
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A. Taratuto — researcher profile on SciRah
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S. Monges×6
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Fabiana Lubieniecki×4

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N. B. Romero — researcher profile on SciRah