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Cytopathologic features of mammary analogue secretory carcinoma

Cancer cytopathology, 2013-05, Vol.121 (5), p.228-233

2013

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Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot

American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2702-2706

2015

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Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblings

American journal of medical genetics. Part A, 2015-05, Vol.167A (5), p.1147-1151

2015

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3q29 interstitial microduplication: A new syndrome in a three-generation family

American journal of medical genetics. Part A, 2008-03, Vol.146A (5), p.601-609

2008

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Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: Search for recurrent chromosome abnormalities

Genes chromosomes & cancer, 2006-04, Vol.45 (4), p.383-391

2006

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Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development

American journal of medical genetics. Part A, 2008-09, Vol.146A (17), p.2293-2297

2008

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Genetic Profiling by Single-Nucleotide Polymorphism-Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma

Brain pathology (Zurich, Switzerland), 2015-03, Vol.25 (2), p.193-201

2015

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An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism

American journal of medical genetics. Part A, 2010-05, Vol.152A (5), p.1318-1321

2010

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An Unbalanced Translocation between Chromosomes 2p and 6p Associated With Axenfeld—Rieger Anomaly ype 3, Hearing Loss, Developmental Delay, and Distinct Facial Dysmorphism

American journal of medical genetics. Part A, 2010, Vol.152 (5), p.1318-1321

2010

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Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

American journal of medical genetics, 1994-11, Vol.53 (3), p.255-263

1994

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An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line

Prenatal diagnosis, 1995-02, Vol.15 (2), p.123-127

1995

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Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization

American journal of medical genetics, 1995-03, Vol.56 (2), p.219-223

1995

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Segregation of a familial balanced (12;10) insertion resulting in dup(10)(q21.2q22.1) and del(10)(q21.2q22.1) in first cousins

American journal of medical genetics, 1997-03, Vol.69 (2), p.188-193

1997

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Chemokines and mitochondrial products activate neutrophils to amplify organ injury during mouse acute liver failure

Hepatology (Baltimore, Md.), 2012-11, Vol.56 (5), p.1971-1982

2012

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Myofibroblastic lesions in the oral cavity: Immunohistochemical and ultrastructural analysis

Oral diseases, 2019-01, Vol.25 (1), p.174-181

2019

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On the catabolism of amino acids in the yeast Dekkera bruxellensis and the implications for industrial fermentation processes

Yeast (Chichester, England), 2018-03, Vol.35 (3), p.299-309

2018

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Complex Methylmercury–Cysteine Alters Mercury Accumulation in Different Tissues of Mice

Basic & clinical pharmacology & toxicology, 2010-10, Vol.107 (4), p.789-792

2010

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Case–contrast study about parent–infant interaction in a Brazilian sample of siblings of children with autism spectrum disorders

Infant mental health journal, 2019-03, Vol.40 (2), p.289-301

2019

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Prospective evaluation of immune haemolysis in liver transplantation

Vox sanguinis, 2020-01, Vol.115 (1), p.72-80

2020

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Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?

Clinical genetics, 2014-02, Vol.85 (2), p.138-146

2014

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Inhibition of melanoma metastasis by dual‐peptide PLGA NPS

Biopolymers, 2017-09, Vol.108 (5), p.n/a

2017

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Microscopical analysis of Candida albicans biofilms on heat-polymerised acrylic resin after chlorhexidine gluconate and sodium hypochlorite treatments

Mycoses, 2011-11, Vol.54 (6), p.e712-e717

2011

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Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

Developmental medicine and child neurology, 2014-11, Vol.56 (11), p.1124-1128

2014

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Study of the cytotoxic and genotoxic potential of the carbonyl ruthenium(II) compound, ct‐[RuCl(CO)(dppb)(bipy)]PF6 [dppb = 1,4‐bis(diphenylphosphino)butane and bipy = 2,2′‐bipyridine], by in vitro and in vivo assays

Journal of applied toxicology, 2019-04, Vol.39 (4), p.630-638

2019

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Study of the cytotoxic and genotoxic potential of the carbonyl ruthenium(II) compound, ct-[RuCl(CO)(dppb)(bipy)]PF 6 [dppb = 1,4-bis(diphenylphosphino)butane and bipy = 2,2'-bipyridine], by in vitro and in vivo assays

Journal of applied toxicology, 2019-04, Vol.39 (4), p.630-638

2019

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Cytopathologic features of mammary analogue secretory carcinoma

Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot

Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblings

3q29 interstitial microduplication: A new syndrome in a three-generation family

Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: Search for recurrent chromosome abnormalities

Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development

Genetic Profiling by Single-Nucleotide Polymorphism-Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma

An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism

An Unbalanced Translocation between Chromosomes 2p and 6p Associated With Axenfeld—Rieger Anomaly ype 3, Hearing Loss, Developmental Delay, and Distinct Facial Dysmorphism

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization

Segregation of a familial balanced (12;10) insertion resulting in dup(10)(q21.2q22.1) and del(10)(q21.2q22.1) in first cousins

Chemokines and mitochondrial products activate neutrophils to amplify organ injury during mouse acute liver failure

Myofibroblastic lesions in the oral cavity: Immunohistochemical and ultrastructural analysis

On the catabolism of amino acids in the yeast Dekkera bruxellensis and the implications for industrial fermentation processes

Complex Methylmercury–Cysteine Alters Mercury Accumulation in Different Tissues of Mice

Case–contrast study about parent–infant interaction in a Brazilian sample of siblings of children with autism spectrum disorders

Prospective evaluation of immune haemolysis in liver transplantation

Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?

Inhibition of melanoma metastasis by dual‐peptide PLGA NPS

Microscopical analysis of Candida albicans biofilms on heat-polymerised acrylic resin after chlorhexidine gluconate and sodium hypochlorite treatments

Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

Study of the cytotoxic and genotoxic potential of the carbonyl ruthenium(II) compound, ct‐[RuCl(CO)(dppb)(bipy)]PF6 [dppb = 1,4‐bis(diphenylphosphino)butane and bipy = 2,2′‐bipyridine], by in vitro and in vivo assays

Study of the cytotoxic and genotoxic potential of the carbonyl ruthenium(II) compound, ct-[RuCl(CO)(dppb)(bipy)]PF 6 [dppb = 1,4-bis(diphenylphosphino)butane and bipy = 2,2'-bipyridine], by in vitro and in vivo assays

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