A.L Taratuto: search on Z-Library

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1

Spastic paraparesis and sensory neuropathy

Silvia N. Tenembaum, Ricardo C. Reisin, Ana L. Taratuto, Natalio Fejerman

Journal:

Year:

1996

Language:

english

File:

PDF, 505 KB

english, 1996

2

Muscle MRI in pediatrics: clinical, pathological and genetic correlation

Cejas, Claudia P., Serra, Maria M., Galvez, David F. Gonzalez, Cavassa, Eliana A., Taratuto, Ana L., Vazquez, Gabriel A., Massaro, Mario E. L., Schteinschneider, Angeles V.

Journal:

Pediatric Radiology

Year:

2017

Language:

english

File:

PDF, 1.92 MB

english, 2017

3

Reinnervation in duchenne muscular dystrophy

Dr. Alberto Dubrovsky, Dr. Ana Lía Taratuto

Journal:

Year:

1983

Language:

english

File:

PDF, 438 KB

english, 1983

4

Letters to the editor

Erich W. Streib, Russell J. M. Lane, Douglass M. Turnbull, Peter Hudgson, Professor Sir John Walton, Roger A. Brumback, Jeffery W. Gerst, John Z. Heckmatt, Victor Dubowitz, Ana Lia Taratuto, Alberto D

Journal:

Year:

1984

Language:

english

File:

PDF, 460 KB

english, 1984

5

Krabbe Disease in Monozygotic Triplets

Hugo A. Arroyo, Jorge Grippo, Analia Taratuto, Jorge Duffau, Nestor Chamoles

Journal:

Developmental Medicine & Child Neurology

Year:

1991

Language:

english

File:

PDF, 297 KB

english, 1991

6

POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardation

Akiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, Sandrine Vuillaumier-Barrot, Nigel Clarke, Sylvie Odent, Diana Rodriguez, Norma B. Romero, Makiko Osawa, Tamao Endo, Taratuto Ana Lia, Nathalie Se

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 284 KB

english, 2009

7

Biopsia muscular en miopatías congénitas y distrofias musculares

Ana Lia Taratuto

Journal:

Neurología Argentina (Elsevier)

Year:

2010

File:

PDF, 604 KB

2010

8

Pompe disease, the must-not-miss diagnosis: A report of 3 patients

Dubrovsky, Alberto, Corderi, Jose, Karasarides, Theodora, Taratuto, Ana Lia

Journal:

Year:

2013

Language:

english

File:

PDF, 570 KB

english, 2013

9

Vasculitic Peripheral Neuropathy, Differences Between Systemic and Non-Systemic Etiologies: A Case Series and Biopsy Report

Castiglione, J.I., Marrodan, M., Alessandro, L., Taratuto, A.L., Brand, P., NoguÃ©s, M., Barroso, F.

Journal:

Journal of Neuromuscular Diseases

Year:

2020

File:

PDF, 406 KB

2020

10

Superficial cerebral astrocytoma attached to dura: Report of six cases in infants

Ana Lía Taratuto, Jorge Monges, Pedro Lylyk, Ramón Leiguarda

Journal:

Year:

1984

Language:

english

File:

PDF, 905 KB

english, 1984

11

Duchenne muscular dystrophy and myotonic dystrophy in the same patient

Alberto L. Dubrovsky, A. L. Taratuto, G. Sevlever, M. Schultz, E. Pegoraro, R. C. Hoop, E. P. Hoffman

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 796 KB

english, 1995

12

Childhood neuronal ceroid-lipofuscinoses in Argentina

Ana Lia Taratuto, María Saccoliti, Gustavo Sevlever, Victor Ruggieri, Hugo Arroyo, María Herrero, Mario Massaro, Natalio Fejerman

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 816 KB

english, 1995

13

Leptomyxid amoeba encephalitis: report of the first case in Argentina

A.L. Taratuto, J. Monges, J.C. Acefe, F. Meli, A. Paredes, A.J. Martinez

Journal:

Transactions of the Royal Society of Tropical Medicine and Hygiene

Year:

1991

Language:

english

File:

PDF, 116 KB

english, 1991

14

Giant axonal neuropathy (GAN): an immunohistochemical and ultrastructural study report of a Latin American case

A. L. Taratuto, G. Sevlever, M. Saccoliti, L. Caceres, M. Schultz

Journal:

Acta Neuropathologica

Year:

1990

Language:

english

File:

PDF, 769 KB

english, 1990

15

Primary rhabdomyosarcoma of brain and cerebellum

A. L. Taratuto, H. A. Molina, B. Diez, G. Zúccaro, J. Monges

Journal:

Acta Neuropathologica

Year:

1985

Language:

english

File:

PDF, 1.98 MB

english, 1985

16

Choroid plexus tumors in infancy and childhood. Focal ependymal differentiation

A. L. Taratuto, H. Molina, J. Monges

Journal:

Acta Neuropathologica

Year:

1983

Language:

english

File:

PDF, 1.02 MB

english, 1983

17

Junín virus encephalitis in mice: Its inhibition by antithymocyte serum

Ana Lía Taratuto, Lidia Z. Tkaczevski, Nora Ruth Nota, Marta R. Nejamkis, Octavio A. Giovanniello

Journal:

Archives of Virology

Year:

1973

Language:

english

File:

PDF, 3.51 MB

english, 1973

18

Subependymal giant cell astrocytoma in children with tuberous sclerosis

Vicente Cuccia, Graciela Zuccaro, Fidel Sosa, Jorge Monges, Fabiana Lubienieky, Ana Lia Taratuto

Journal:

Child's Nervous System

Year:

2003

Language:

english

File:

PDF, 371 KB

english, 2003

19

Extratemporal epilepsy in children: candidate selection and surgical treatment

H. B. Pomata, R. González, M. Bartuluchi, C. A. Petre, C. Ciraolo, R. Caraballo, R. Cersósimo, S. Tenembaum, A. M. Soprano, C. S. Medina, A. Rabinowicz, H. Waisburg, A. L. Taratuto, A. Taratuto, J. Mo

Journal:

Child's Nervous System

Year:

2000

Language:

english

File:

PDF, 149 KB

english, 2000

20

Characterization of brain tumors by MRS, DWI and Ki-67 labeling index

J. A. Calvar, F. J. Meli, C. Romero, M. L. Calcagno P. Yánez, A. R. Martinez, H. Lambre, A. L. Taratuto, G. Sevlever

Journal:

Journal of Neuro-Oncology

Year:

2005

Language:

english

File:

PDF, 319 KB

english, 2005

21

Loss of heterozygosity at 1p-19q induces a global change in oligodendroglial tumor gene expression

Rubén Ferrer-Luna, Manuel Mata, Lina Núñez, Jorge Calvar, Francisco Dasí, Eugenia Arias, José Piquer, Miguel Cerdá-Nicolás, Ana Lía Taratuto, Gustavo Sevlever, Bernardo Celda, Horacio Martinetto

Journal:

Journal of Neuro-Oncology

Year:

2009

Language:

english

File:

PDF, 477 KB

english, 2009

22

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

J. A. Bevilacqua, N. Monnier, M. Bitoun, B. Eymard, A. Ferreiro, S. Monges, F. Lubieniecki, A. L. Taratuto, A. Laquerrière, K. G. Claeys, I. Marty, M. Fardeau, P. Guicheney, J. Lunardi, N. B. Romero

Journal:

Neuropathology and Applied Neurobiology

Year:

2011

Language:

english

File:

PDF, 1.83 MB

english, 2011

23

Trichinosis

Ana Lia Taratuto, Stella M. Venturiello

Journal:

Brain Pathology

Year:

1997

Language:

english

File:

PDF, 5.56 MB

english, 1997

24

Echinococcosis

Ana Lia Taratuto, Stella M. Venturiello

Journal:

Brain Pathology

Year:

1997

Language:

english

File:

PDF, 2.73 MB

english, 1997

25

Diagnosis of mitochondrial disorders applying massive pyrosequencing

Marcelo Andrés Kauffman, Dolores González-Morón, Damián Consalvo, Gastón Westergaard, Martín Vazquez, Estefanía Mancini, Ana Lía Taratuto, Raúl Rey, Silvia Kochen

Journal:

Molecular Biology Reports

Year:

2012

Language:

english

File:

PDF, 283 KB

english, 2012

26

Trypanosoma cruzi: Experimental immunization of mice

J.F. Yanovsky, O.C. Traversa, A.L. Taratuto, G.A. Schumnis, S.M. González Cappa, A.S. Parodi

Journal:

Experimental Parasitology

Year:

1969

Language:

english

File:

PDF, 4.27 MB

english, 1969

27

PS-54-8 Familial bulbospinal neuronopathy affecting both sexes

Guillermo Paradiso, Federico Micheli, Ana Lía Taratuto, Ignacio Casas Parera

Journal:

Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control

Year:

1995

Language:

english

File:

PDF, 124 KB

english, 1995

28

Genetic prion disease with codon 196 PRNP mutation: clinical and pathological findings

Gabi Schelzke, Sabina Eigenbrod, Carlos Romero, Daniela Varges, Maren Breithaupt, Ana L. Taratuto, Hans A. Kretzschmar, Inga Zerr

Journal:

Neurobiology of Aging

Year:

2011

Language:

english

File:

PDF, 993 KB

english, 2011

29

G.P.8 12 Centronuclear myopathy: clinical and morphological phenotype/genotype correlations

J.A. Bevilacqua, M. Bitoun, A. Oldfors, F. Lubieniecki, S. Monges, A.L. Taratuto, A. Urtizberea, L. Cartier, E. Uro-Coste, C. Cances, M. Fardeau, P. Guicheney, N.B. Romero

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 45 KB

english, 2006

30

G.P.6 09 Normal distribution of Ins(1,4,5)P3 receptors is disrupted in Duchenne muscular dystrophy

J.A. Bevilacqua, C. Cardenas, R. Figueroa, A.L. Taratuto, J. Molgó, E. Jaimovich

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 57 KB

english, 2006

31

G.O. 10 Dynamin 2 mutations and impairment of EGF-induced MAPK activation

M. Bitoun, J.A. Bevilacqua, B. Prudhon, S. Maugenre, F. Lubieniecki, S. Monges, A.L. Taratuto, M. Fardeau, B. Eymard, E. Uro-Coste, N.B. Romero, P. Guicheney

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 47 KB

english, 2006

32

G.P.5.01 Inflammatory or ‘congenital myopathy’ type findings in muscle biopsies of patients with LMNA mutations

F. Lubieniecki, S. Monges, A. Dubrovsky, A. Stewart-Harris, V. Ruggieri, F. Barroso, G. Espada, M. Ferrea, M. Robertella, P. Richard, G. Bonne, N. Romero, P. Guicheney, M. Sacolitti, A. Taratuto

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 49 KB

english, 2007

33

G.P.8.09 Exercise intolerance and rippling syndrome in caveolinopathy

F. Barroso, M. Nogués, R. Leiguarda, A. Taratuto

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 60 KB

english, 2007

34

C.P.2.14 Merosin-deficient congenital muscular dystrophy: Analysis of 7 patients

R. Erazo, M. Schultz, A. Taratuto, A. Wicki, M. Pimstein, A. Henríquez, E. Bertini, J. Carrasco, G. Bascuñán, E. Rodillo, J. Latorre

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 49 KB

english, 2007

35

C.P.4.11 Ragged red fibres finding in muscle biopsy of dynamin 2-related centronuclear myopathy

L. Pirra, A. Dubrovsky, M. Bitoun, P. Guicheney, N. Romero, M. Sacolitti, A. Taratuto

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 61 KB

english, 2007

36

C.P.4.09 Dynamin 2 mutations in the pleckstrin homology domain cause severe neonatal centronuclear myopathy

M. Bitoun, J. Bevilacqua, B. Prudhon, A. Taratuto, S. Monges, F. Lubieniecki, C. Cances, E. Uro-Coste, M. Mayer, M. Fardeau, P. Guicheney, N. Romero

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 46 KB

english, 2007

37

D.P.1.11 Saethre-Chotzen syndrome: A severe case of Facioscapulohumeral Muscular Dystrophy (FSHD) in a patient

S. Monges, M. Torrado, J. Castaño, A.L. Taratuto, C.A. Bacino, E.D. Corona, F. Lubieniecki, A.L. Rosa

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 62 KB

english, 2008

38

G.P.16.04. Branching enzyme deficiency should be considered in the differential diagnosis of severe congenital hypotonia

A.L. Taratuto, H.O. Akman, M. Saccoliti, M. Riudavets, N. Arakaki, M. Fernández, L. Mesa, G. Sevlever, H. Goebel, S. Di Mauro

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 46 KB

english, 2008

39

G.P.1.07 Progressive muscle biopsies morphological changes in long-term follow-up of multiminicore disease related to RYR1 gene

A.L. Taratuto, M. Saccoliti, F. Lubieniecki, N. Monnier, N. Romero, P. Richard, J. Lunardi

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 40 KB

english, 2009

40

G.P.8.03 Misleading muscle biopsies in late onset Pompe’s disease

A.L. Taratuto, A. Dubrovsky, J. Corderi

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 50 KB

english, 2009

41

G.P.12.06 Progressive muscle biopsies morphological changes in MTM1-related centronuclear congenital myopathy

F. Lubieniecki, V. Biancalana, N. Romero, S. Monges, M. Saccoliti, A.L. Taratuto

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 39 KB

english, 2009

42

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.L. Taratuto, H.O. Akman, M. Saccoliti, M. Riudavets, N. Arakaki, L. Mesa, G. Sevlever, H. Goebel, S. DiMauro

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 1.71 MB

english, 2010

43

P2.9 LMNA-related congenital muscular dystrophy: Clinical, pathological and molecular findings

M.S. Monges, F. Lubieniecki, S. Quijano-Roy, M. Saccoliti, N.B. Romero, P. Richard, A.L. Taratuto

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

44

P2.10 A new form of congenital muscular dystrophy with subsarcolemmal inclusions arising from disintegrated myonuclei

A.L. Taratuto, I. Nelson, M. Olivé, H. Waisburg, M. Saccoliti, M. Beuvin, D. Chauveau, P. Richard, T. Voit, G. Bonne, N.B. Romero

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 61 KB

english, 2011

45

P3.36. Phenotypic spectrum in myopathies with tubular aggregates

F. Funk, C. Ceuterick-de Groote, J.J. Martin, A. Meinhardt, J. de Bleecker, P. de Jonghe, A.L. Taratuto, M. Saccoliti, J.M. Schröder, J.B. Schulz, J. Weis, K.G. Claeys

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 65 KB

english, 2011

46

New Proteins Configure a Brain Drug Resistance Map in Tuberous Sclerosis

Alberto J. Lazarowski, Fabiana J. Lubieniecki, Sandra A. Camarero, Hugo H. Pomata, Marcelo A. Bartuluchi, Gustavo Sevlever, Ana Lía Taratuto

Journal:

Pediatric Neurology

Year:

2006

Language:

english

File:

PDF, 349 KB

english, 2006

47

Multidrug resistance proteins in tuberous sclerosis and refractory epilepsy

Alberto Lazarowski, Fabiana Lubieniecki, Sandra Camarero, Hugo Pomata, Marcelo Bartuluchi, Gustavo Sevlever, Ana Lía Taratuto

Journal:

Pediatric Neurology

Year:

2004

Language:

english

File:

PDF, 208 KB

english, 2004

48

Tuberous sclerosis associated with MDR1 gene expression and drug-resistant epilepsy

Alberto Lazarowski, Gustavo Sevlever, Analı́a Taratuto, Mario Massaro, Adrián Rabinowicz

Journal:

Pediatric Neurology

Year:

1999

Language:

english

File:

PDF, 128 KB

english, 1999

49

Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular–eye–brain loci: report of three siblings

V Ruggieri, F Lubieniecki, F Meli, D Diaz, E Ferragut, K Saito, M Brockington, F Muntoni, Y Fukuyama, A.L Taratuto

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 5.33 MB

english, 2001

50

Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study

A.L Taratuto, F Lubieniecki, D Dı́az, M Schultz, V Ruggieri, M Saccoliti, A Dubrovsky

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 3.53 MB

english, 1999

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