I. Szijan

S. Baranzini, I. Szijan, D. Parma, 1998, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum.

S. Baranzini, J. Cresto, N. Chamoles, 1997, American journal of medical genetics.

Supernumerary marker 15 chromosome in a patient with Prader–Willi syndrome

S. Esperante, V. Ferreiro, I. Szijan, 2004, Clinical genetics.

Small mutation screening in the DMD gene by whole exome sequencing of an Argentine Duchenne/Becker muscular dystrophies cohort

C. Mazzanti, I. Szijan, F. Giliberto, 2018, Neuromuscular Disorders.

RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling

I. Szijan, D. Parma, F. Giliberto, 2017, PloS one.

Recurrent Somatic Chromosomal Abnormalities in Relapsed Extraocular Retinoblastoma

J. Mora, F. Radvanyi, O. Podhajcer, 2021, Cancers.

Neurofibromatosis type 2: Molecular and clinical analyses in Argentine sporadic and familial cases

V. Ferreiro, I. Szijan, A. Basso, 2010, Neuroscience Letters.

The influence of estrogen administration on the subcellular receptors distribution and its biological effect in the rat anterior pituitary gland.

M. Romano, I. Szijan, J. Burdman, 1983, Journal of steroid biochemistry.

Gene Expression Profiling of ErbB Receptors and Ligands in Human Meningiomas

I. Salmon, I. Bièche, M. Vidaud, 2009, Cancer investigation.

Analysis of complex structural variants in the DMD gene in one family

P. Lapunzina, J. Nevado, C. Mazzanti, 2020, Neuromuscular Disorders.

Expression of p16INK4A gene in human pituitary tumours

O. Bruno, A. Paes de Lima, I. Szijan, 2007, Pituitary.

Molecular diagnosis of dystrophinopathies using a multi‐technique analysis algorithm

I. Szijan, Daniela Ottaviani, J. Cotignola, 2014, Muscle & nerve.

Detection of germline mosaicism in two duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene

V. Ferreiro, I. Szijan, F. Giliberto, 2012, Molecular Diagnosis.

The Role of Polymorphic Short Tandem (CA)n Repeat Loci Segregation Analysis in the Detection of Duchenne Muscular Dystrophy Carriers and Prenatal Diagnosis

V. Ferreiro, I. Szijan, F. Giliberto, 2012, Molecular Diagnosis.

Carrier detection in Duchenne and Becker muscular dystrophy Argentine families

S. Baranzini, I. Szijan, V. Dalamón, 1998, Clinical genetics.

Gene Expression Profiling of the Hedgehog Signaling Pathway in Human Meningiomas

I. Salmon, I. Bièche, M. Vidaud, 2010, Molecular medicine.

Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation.

V. Ferreiro, I. Szijan, V. Dalamón, 2004, Journal of biochemistry and molecular biology.

Studies on estrogen receptors in the cytosol and nuclei of the rat anterior pituitary gland. Determination of specific sites by [3H]-estradiol exchange assay.

I. Szijan, J. Burdman, G. Alonso, 1981, Journal of steroid biochemistry.

Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion

D. Marzese, V. Ferreiro, I. Szijan, 2009, Muscle & nerve.

Four new polymorphisms in the human dystrophin gene from an Argentinian population

S. Baranzini, I. Szijan, A. Speer, 1997, Muscle & nerve.

NF2 Tumor suppressor gene

C. Bruder, J. Dumanski, G. Rouleau, 2007, NeuroMolecular Medicine.

A Comprehensive and Efficient Detection of Somatic Mutations by Denaturing HPLC and Microarray-CGH

C. Bruder, J. Dumanski, G. Rouleau, 2003 .

RB1 Germ-Line Deletions in Argentine Retinoblastoma Patients

V. Ferreiro, I. Szijan, V. Dalamón, 2012, Molecular Diagnosis & Therapy.

Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.

I. Szijan, Daniela Ottaviani, C. Alonso, 2015, Medicina.

Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.

V. Ferreiro, I. Szijan, V. Dalamón, 2004, Neurological research.

Effect of histones from brain on DNA-synthesis in vitro

I. Szijan, G. Jahn, J. Burdman, 1977, Experientia.

EFFECT OF ACIDIC DEOXYRIBONUCLEOPROTEINS FROM BRAIN ON DNA SYNTHESIS IN VITRO

I. Szijan, J. Burdman, 1976, Journal of neurochemistry.

DNA polymerase activity in fractions from brain cell nuclei.

I. Szijan, J. Burdman, 1974, Brain Research.

EARLY EVENTS IN THE EFFECT OF HYDROCORTISONE ACETATE ON DNA REPLICATION IN THE RAT BRAIN

I. Szijan, G. Jahn, J. A. Burdman, 1975, Journal of neurochemistry.

Spectrum of RB1 Mutations in Argentine Patients: 20-years Experience in the Molecular Diagnosis of Retinoblastoma

G. Chantada, I. Szijan, D. Parma, 2013, Ophthalmic genetics.

NUCLEAR PROTEINS IN BRAIN OF 7‐DAY‐OLD AND ADULT RATS

I. Szijan, J. Burdman, 1973, Journal of neurochemistry.

Minimal disseminated disease evaluation and outcome in trilateral retinoblastoma

D. Alonso, J. Rossi, G. Chantada, 2018, British Journal of Ophthalmology.

Prognostic value of mutations in isocitrate dehydrogenase 1 (IDH1) and reverse telomerase transcriptase (TERT) in Argentine patients` gliomas

I. Szijan, D. Parma, F. Giliberto, 2021 .

Expression of c-myc and c-fos oncogenes in different rat brain regions during postnatal development

I. Szijan, D. Parma, S. Benasayag, 1991, International Journal of Developmental Neuroscience.

Gene Expression Profiling of the Hedgehog Signaling Pathway in Human Meningiomas

I. Salmon, I. Bièche, M. Vidaud, 2010, Molecular medicine.

Alterations in the retinoblastoma pathway of cell cycle control in parathyroid tumors.

C. Cordon-Cardo, I. Orlow, N. Mezzadri, 2000, Oncology Report.

Genotypic and phenotypic characterization of the histoblood group ABO(H) in primary bladder tumors

C. Cordon-Cardo, Zuo-Feng Zhang, L. Lacombe, 1998, International journal of cancer.

Neurofibromatosis type 2: Molecular and clinical analyses in Argentine sporadic and familial cases

V. Ferreiro, I. Szijan, A. Basso, 2010, Neuroscience Letters.