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Specific features to differentiate Giant cell arteritis aortitis from aortic atheroma using FDG-PET/CT

Scientific reports, 2021-08, Vol.11 (1), p.17389-17389, Article 17389

2021

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ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

Nature communications, 2020-01, Vol.11 (1), p.198-14, Article 198

2020

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Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

Nature genetics, 2003-04, Vol.33 (4), p.459-461

2003

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Early skin-to-skin contact and risk of late-onset-sepsis in very and extremely preterm infants

Pediatric research, 2023-06, Vol.93 (7), p.2091-2100

2023

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Adjuvant dendritic cell therapy in stage IIIB/C melanoma: the MIND-DC randomized phase III trial

Nature communications, 2024-02, Vol.15 (1), p.1632-1632, Article 1632

2024

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Mediator contributes to IgH locus VDJ rearrangements by promoting usage of most distal V segments

Cellular & molecular immunology, 2020-04, Vol.17 (4), p.407-409

2020

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Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Molecular psychiatry, 2022-11, Vol.27 (11), p.4453-4463

2022

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IgH locus suicide recombination does not depend on NHEJ in contrast to CSR in B cells

Cellular & molecular immunology, 2019-02, Vol.16 (2), p.201-202

2019

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Stimulation of the β3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Neuropsychopharmacology (New York, N.Y.), 2007-04, Vol.33 (3), p.574-587

2007

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Author Correction: Tree mode of death and mortality risk factors across Amazon forests

Nature communications, 2021-01, Vol.12 (1), p.209-2, Article 209

2021

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Bayesian blacksmithing: discovering thermomechanical properties and deformation mechanisms in high-entropy refractory alloys

npj computational materials, 2024-07, Vol.10 (1), p.164-13, Article 164

2024

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Germline deletion of the miR-1792 cluster causes skeletal and growth defects in humans

Nature genetics, 2011-10, Vol.43 (10), p.1026-1030

2011

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Germline deletion of the miR-17-92 cluster causes growth and skeletal defects in humans

Nature genetics, 2011-09, Vol.43 (10), p.1026-1030

2011

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Dissection of the MYCN locus in Feingold Syndrome and isolated esophageal atresia

European journal of human genetics : EJHG, 2011-01

2011

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Genetics and Early Disturbances of Breathing Control: The Genetics of Childhood Disease and Development: A Series of Review Articles

Pediatric research, 2004-05, Vol.55 (5), p.729-733

2004

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Stimulation of the [beta]3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Neuropsychopharmacology (New York, N.Y.), 2008-02, Vol.33 (3), p.574

2008

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Stimulation of the beta3-Adrenoceptor as a novel treatment strategy for anxiety and depressive disorders

Neuropsychopharmacology (New York, N.Y.), 2008-02, Vol.33 (3), p.574

2008

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Treatment with recombinant human growth hormone in short children with nephropathic cystinosis : No evidence for increased deterioration rate of renal function

Pediatric research, 1998-04, Vol.43 (4), p.484-488

1998

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WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1in most invasive carcinomas except of the medullary type

Oncogene, 2001-09, Vol.20 (41), p.5810

2001

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Impact of Postnatal Dexamethasone (DEX) on the Incidence and Severity of Retinopathy of Prematurity (ROP) in the Surfactant Era

Pediatric research, 1999-04, Vol.45 (4, Part 2 of 2), p.183-183A

1999

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Jaundice Associated With Hypertrophic Pyloric Stenosis Is An Early Manifestation of Gilbert Disease

Pediatric research, 1998-09, Vol.44 (3), p.425-425

1998

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133 CEREBELLAR INVOLVEMENT IN BILIRUBIN ENCEPHALOPATHY DUE TO CRIGLER-NAJJAR TYPE 1 DISEASE

Pediatric research, 1991-12, Vol.30 (6), p.650-650

1991

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Specific features to differentiate Giant cell arteritis aortitis from aortic atheroma using FDG-PET/CT

ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

Early skin-to-skin contact and risk of late-onset-sepsis in very and extremely preterm infants

Adjuvant dendritic cell therapy in stage IIIB/C melanoma: the MIND-DC randomized phase III trial

TMPRSS2 is a functional receptor for human coronavirus HKU1

Mediator contributes to IgH locus VDJ rearrangements by promoting usage of most distal V segments

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

IgH locus suicide recombination does not depend on NHEJ in contrast to CSR in B cells

Stimulation of the β3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Neurochemical, electrophysiological and pharmacological profiles of the selective inhibitor of the glycine transporter-I SSR504734, a potential new type of antipsychotic

Author Correction: Tree mode of death and mortality risk factors across Amazon forests

Bayesian blacksmithing: discovering thermomechanical properties and deformation mechanisms in high-entropy refractory alloys

Germline deletion of the miR-1792 cluster causes skeletal and growth defects in humans

Germline deletion of the miR-17-92 cluster causes growth and skeletal defects in humans

Dissection of the MYCN locus in Feingold Syndrome and isolated esophageal atresia

Genetics and Early Disturbances of Breathing Control: The Genetics of Childhood Disease and Development: A Series of Review Articles

Stimulation of the [beta]3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Stimulation of the beta3-Adrenoceptor as a novel treatment strategy for anxiety and depressive disorders

Treatment with recombinant human growth hormone in short children with nephropathic cystinosis : No evidence for increased deterioration rate of renal function

WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1in most invasive carcinomas except of the medullary type

Impact of Postnatal Dexamethasone (DEX) on the Incidence and Severity of Retinopathy of Prematurity (ROP) in the Surfactant Era

Jaundice Associated With Hypertrophic Pyloric Stenosis Is An Early Manifestation of Gilbert Disease

133 CEREBELLAR INVOLVEMENT IN BILIRUBIN ENCEPHALOPATHY DUE TO CRIGLER-NAJJAR TYPE 1 DISEASE

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