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Overview of the MODARIA programme (and comments on implications for future programmes of work)

Journal of radiological protection, 2022-06, Vol.42 (2), p.20505

2022

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The IAEA handbook on radionuclide transfer to wildlife

Journal of environmental radioactivity, 2013-07, Vol.121, p.55-74

2013

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Radiological Protection of the Environment and its Implementation into IAEA Safety Standards

Atom Indonesia, 2013-12, Vol.39 (3), p.101-105

2013

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Use of the ICRP system for the protection of marine ecosystems

Annals of the ICRP, 2015-06, Vol.44 (1_suppl), p.304-312

2015

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Overview of the MODARIA programme (and comments on implications for future programmes of work) The IAEA wishes to express its gratitude to all those who participated in the work of both phases of the MODARIA programme and gratefully acknowledges the valuable contributions of all those who contributed to the preparation of the outputs

Journal of radiological protection, 2022-03, Vol.42 (2)

2022

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Genetic and epigenetic profile of sporadic pheochromocytomas

Journal of medical genetics, 2004-03, Vol.41 (3), p.e30-30

2004

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SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation

Journal of medical genetics, 2002-10, Vol.39 (10), p.e64-64

2002

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A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

The New England journal of medicine, 2002-01, Vol.346 (4), p.243-249

2002

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Investigation of the importance of site-specific fauna in environmental risk assessment for routine atmospheric radionuclides releases

The Science of the total environment, 2018

2018

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Findings and recommendations from an international comparison of models and approaches for the estimation of radiological exposure to non-human biota

Radioprotection, 2009, Vol.44 (5), p.565-570

2009

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Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss

Journal of medical genetics, 2002-07, Vol.39 (7), p.502-506

2002

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Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients

Journal of medical genetics, 2003-05, Vol.40 (5), p.e72-72

2003

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Angiotensin-converting enzyme gene polymorphism and antiproteinuric response to renoprotective therapy

Nephrology, dialysis, transplantation, 1998-04, Vol.13 (4), p.1050-1051

1998

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Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma

European journal of human genetics : EJHG, 2002-08, Vol.10 (8), p.457-461

2002

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Screening for mutations in the steroidogenic acute regulatory protein and steroidogenic factor-1 genes, and in CYP11A and dosage-sensitive sex reversal-adrenal hypoplasia gene on the X chromosome, gene-1 (DAX-1), in hyperandrogenic hirsute women

The journal of clinical endocrinology and metabolism, 2001-04, Vol.86 (4), p.1746-1749

2001

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Insulin gene variable number of tandem repeats regulatory polymorphism is not associated with hyperandrogenism in Spanish women

Fertility and sterility, 2002-04, Vol.77 (4), p.666-668

2002

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Reference methodologies for radioactive controlled discharges an activity within the IAEA’s program environmental modelling for radiation safety II (EMRAS II)

Radioprotection, 2011, Vol.46 (Supplément), p.S687-S693

2011

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G12S and H50R variations are polymorphisms in the SDHD gene

Genes chromosomes & cancer, 2003-06, Vol.37 (2), p.220-221

2003

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Outcomes of Limited Open Achilles Repair Using Modified Ring Foreceps

Foot & ankle orthopaedics, 2017-09, Vol.2 (3), p.2473011417

2017

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Prevalence of Vitamin D Deficiency in Patients with Talar Osteochondral Lesions

Foot & ankle orthopaedics, 2018-07, Vol.3 (3), p.2473011418

2018

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Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease

Kidney international, 1999-07, Vol.56 (1), p.28-33

1999

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Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations

Human mutation, 2004-02, Vol.23 (2), p.160-169

2004

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The EUROGEM map of human chromosome 5

European journal of human genetics : EJHG, 1994, Vol.2 (3), p.212-213

1994

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Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene

Human genetics, 1997-12, Vol.101 (2), p.229-234

1997

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Dinucleotide repeat polymorphism at the D4S2458 locus close to the PKD2 locus on human chromosome 4q

Human genetics, 1995-05, Vol.95 (5), p.601-602

1995

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Overview of the MODARIA programme (and comments on implications for future programmes of work)

The IAEA handbook on radionuclide transfer to wildlife

Radiological Protection of the Environment and its Implementation into IAEA Safety Standards

Use of the ICRP system for the protection of marine ecosystems

Genetic and epigenetic profile of sporadic pheochromocytomas

SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation

A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

Investigation of the importance of site-specific fauna in environmental risk assessment for routine atmospheric radionuclides releases

Findings and recommendations from an international comparison of models and approaches for the estimation of radiological exposure to non-human biota

Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients

Angiotensin-converting enzyme gene polymorphism and antiproteinuric response to renoprotective therapy

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma

Screening for mutations in the steroidogenic acute regulatory protein and steroidogenic factor-1 genes, and in CYP11A and dosage-sensitive sex reversal-adrenal hypoplasia gene on the X chromosome, gene-1 (DAX-1), in hyperandrogenic hirsute women

Insulin gene variable number of tandem repeats regulatory polymorphism is not associated with hyperandrogenism in Spanish women

Reference methodologies for radioactive controlled discharges an activity within the IAEA’s program environmental modelling for radiation safety II (EMRAS II)

G12S and H50R variations are polymorphisms in the SDHD gene

Outcomes of Limited Open Achilles Repair Using Modified Ring Foreceps

Prevalence of Vitamin D Deficiency in Patients with Talar Osteochondral Lesions

Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease

Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations

The EUROGEM map of human chromosome 5

Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene

Dinucleotide repeat polymorphism at the D4S2458 locus close to the PKD2 locus on human chromosome 4q

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