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Different postharvest strategies to preserve broccoli quality during storage and shelf life: Controlled atmosphere and 1-MCP

Food chemistry, 2013-05, Vol.138 (1), p.564-573

2013

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NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases

Human genetics, 2021-12, Vol.140 (12), p.1665-1678

2021

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SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions

British journal of ophthalmology, 2007-11, Vol.91 (11), p.1471-1476

2007

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Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

Clinical genetics, 2008-04, Vol.73 (4), p.360-366

2008

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Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Journal of medical genetics, 2003-07, Vol.40 (7), p.e89-89

2003

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Preoperative Staging and Tumor Resectability Assessment of Pancreatic Cancer: Prospective Study Comparing Endoscopic Ultrasonography, Helical Computed Tomography, Magnetic Resonance Imaging, and Angiography

The American journal of gastroenterology, 2004-03, Vol.99 (3), p.492-501

2004

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

American journal of human genetics, 2012-09, Vol.91 (3), p.527-532

2012

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Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma

Prenatal diagnosis, 2002-10, Vol.22 (10), p.946-948

2002

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Pulmonary function tests and CT scan in the management of idiopathic pulmonary fibrosis

American journal of respiratory and critical care medicine, 1998-08, Vol.158 (2), p.431-436

1998

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Increased risk of tumor seeding after percutaneous radiofrequency ablation for single hepatocellular carcinoma

Hepatology (Baltimore, Md.), 2001-05, Vol.33 (5), p.1124-1129

2001

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Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families

Human mutation, 2001, Vol.17 (1), p.80-80

2001

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PHENIX measurements of low momentum direct photon radiation

Nuclear physics. A, 2019-02, Vol.982, p.763-766

Khachatryan, Vladimir

2019

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Interleukin-8 expression in bronchoalveolar lavage cells in the evaluation of alveolitis in idiopathic pulmonary fibrosis

Respiratory medicine, 1998-02, Vol.92 (2), p.338-344

1998

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Randomized controlled trial of interferon treatment for advanced hepatocellular carcinoma

Hepatology (Baltimore, Md.), 2000-01, Vol.31 (1), p.54-58

2000

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Prenatal diagnosis on fetal cells from maternal blood: practical comparative evaluation of the first and second trimesters

Prenatal diagnosis, 2001-03, Vol.21 (3), p.165-170

2001

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Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

Nature genetics, 1998-01, Vol.18 (1), p.11-12

1998

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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice

Human molecular genetics, 2002-03, Vol.11 (5), p.547-557

2002

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Prenatal diagnosis on fetal cells obtained from maternal peripheral blood: Report of 66 cases

Prenatal diagnosis, 1999-10, Vol.19 (10), p.934-940

1999

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On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa

Human molecular genetics, 2004-03, Vol.13 (6), p.641-650

2004

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Treatment of small hepatocellular carcinoma in cirrhotic patients: A cohort study comparing surgical resection and percutaneous ethanol injection

Hepatology (Baltimore, Md.), 1993-11, Vol.18 (5), p.1121-1126

1993

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Natural history of untreated nonsurgical hepatocellular carcinoma: Rationale for the design and evaluation of therapeutic trials

Hepatology (Baltimore, Md.), 1999-01, Vol.29 (1), p.62-67

1999

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Calcifications in the portal venous system: comparison of plain films, sonography, and CT

American journal of roentgenology (1976), 1992-08, Vol.159 (2), p.321

1992

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The Genetic Basis of the Pierre Robin Sequence

The Cleft palate-craniofacial journal, 2006-03, Vol.43 (2), p.155-159

2006

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Tumor size determines the efficacy of percutaneous ethanol injection for the treatment of small hepatocellular carcinoma

Hepatology (Baltimore, Md.), 1992-08, Vol.16 (2), p.353-357

1992

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Different postharvest strategies to preserve broccoli quality during storage and shelf life: Controlled atmosphere and 1-MCP

NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions

Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Preoperative Staging and Tumor Resectability Assessment of Pancreatic Cancer: Prospective Study Comparing Endoscopic Ultrasonography, Helical Computed Tomography, Magnetic Resonance Imaging, and Angiography

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma

Pulmonary function tests and CT scan in the management of idiopathic pulmonary fibrosis

Increased risk of tumor seeding after percutaneous radiofrequency ablation for single hepatocellular carcinoma

Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families

PHENIX measurements of low momentum direct photon radiation

Interleukin-8 expression in bronchoalveolar lavage cells in the evaluation of alveolitis in idiopathic pulmonary fibrosis

Randomized controlled trial of interferon treatment for advanced hepatocellular carcinoma

Prenatal diagnosis on fetal cells from maternal blood: practical comparative evaluation of the first and second trimesters

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice

Prenatal diagnosis on fetal cells obtained from maternal peripheral blood: Report of 66 cases

On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa

Treatment of small hepatocellular carcinoma in cirrhotic patients: A cohort study comparing surgical resection and percutaneous ethanol injection

Natural history of untreated nonsurgical hepatocellular carcinoma: Rationale for the design and evaluation of therapeutic trials

Calcifications in the portal venous system: comparison of plain films, sonography, and CT

The Genetic Basis of the Pierre Robin Sequence

Tumor size determines the efficacy of percutaneous ethanol injection for the treatment of small hepatocellular carcinoma

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