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HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome

Frontiers in genetics, 2023-03, Vol.14, p.1137767

2023

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A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases

Scientific reports, 2017-12, Vol.7 (1), p.17641-9, Article 17641

2017

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Innovative PCR without DNA extraction for African sickle cell disease diagnosis

Hematology (Luxembourg), 2018-03, Vol.23 (3), p.181-186

2018

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Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies

Molecular genetics and metabolism, 2014-12, Vol.113 (4), p.307-314

2014

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Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome

Molecular genetics and metabolism, 2018-05, Vol.124 (1), p.87-93

2018

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The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

Clinical genetics, 2010-11, Vol.78 (5), p.457-463

2010

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Tryptophan catabolism differentiates breast cancer patients from healthy controls but does not predict outcome

Annals of oncology, 2019-05, Vol.30, p.iii18-iii18

2019

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An insertion–deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases

Human molecular genetics, 2007-12, Vol.16 (24), p.3008-3016

2007

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NF-κB2/p100 induces Bcl-2 expression

Leukemia, 2003-07, Vol.17 (7), p.1349-1356

2003

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GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

Hormone and metabolic research, 2016-06, Vol.48 (6), p.389

2016

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ATP‐gated P2X1 ion channels protect against endotoxemia by dampening neutrophil activation

Journal of thrombosis and haemostasis, 2012-03, Vol.10 (3), p.453-465

2012

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159 Neoadjuvant chemotherapy in breast cancer patients induces expression of miR-34a and miR-122

European journal of cancer (1990), 2014-11, Vol.50, p.53-54

2014

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Transcriptional activation of cyclooxygenase-2 by tumor suppressor p53 requires nuclear factor-kappaB

Oncogene, 2006-09, Vol.25 (42), p.5708-5718

2006

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Involvement of Iκbζ in glioblastomas and its potential implication in radioresistance

European journal of cancer (1990), 2016-12, Vol.69, p.S21-S21

2016

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P‐035: RED BLOOD CELL ALLOIMMUNIZATION IN SICKLE CELL DISEASE PATIENTS IN THE DEMOCRATIC REPUBLIC OF THE CONGO

HemaSphere, 2022-08, Vol.6 (Suppl), p.34-34

2022

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New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes

Facts, views & vision in ObGyn, 2016-09, Vol.8 (3), p.161-167

2016

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Hypogonadisme hypogonadotrope anosmique associé à une nouvelle mutation hétérozygote c.937C>T, p.His314Tyr de l’isoforme IIIb du gène FGFR1

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.313-313

2016

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Increased expression of receptor activator of NF‐κB ligand (RANKL), its receptor RANK and its decoy receptor osteoprotegerin in the colon of Crohn's disease patients

Clinical and experimental immunology, 2004-12, Vol.138 (3), p.491-498

2004

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Mechanisms of persistent NF-kappa B activity in the bronchi of an animal model of asthma

The Journal of immunology (1950), 2000-11, Vol.165 (10), p.5822-5830

2000

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Caractérisation clinique, neuroendocrinienne, génétique et résultats thérapeutiques dans le syndrome de Kallmann et de l’hypogonadisme normosmique idiopathique : expérience liégeoise

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.314-314

2016

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O9.06 PROGNOSTIC RELEVANCE AND ONCOGENIC CORRELATES OF EPILEPSY IN GLIOBLASTOMA PATIENTS

Neuro-oncology (Charlottesville, Va.), 2014-09, Vol.16 (suppl 2), p.ii21-ii21

2014

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Hypogonadisme hypogonadotrope normosmique familial : identification d’une nouvelle mutation c.1664-2A > T du gène FGFR1

Annales d'endocrinologie, 2015-09, Vol.76 (4), p.366-366

2015

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Étude moléculaire du gène AIP sur plus de 1400 individus atteints d’adénome hypophysaire

Annales d'endocrinologie, 2015-09, Vol.76 (4), p.351-352

2015

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Une forme compliquée d’hypercalcémie hypocalciurique familiale

Annales d'endocrinologie, 2015-09, Vol.76 (4), p.488-488

2015

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44P Role of DNA methylation and non-coding RNA in INK4b-ARF-INK4a locus expression

Annals of oncology, 2020-09, Vol.31, p.S257-S257

2020

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HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome

A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases

Innovative PCR without DNA extraction for African sickle cell disease diagnosis

Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies

Genetic assessment and folate receptor autoantibodies in infantile-onset cerebral folate deficiency (CFD) syndrome

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

Tryptophan catabolism differentiates breast cancer patients from healthy controls but does not predict outcome

An insertion–deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases

NF-κB2/p100 induces Bcl-2 expression

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

ATP‐gated P2X1 ion channels protect against endotoxemia by dampening neutrophil activation

159 Neoadjuvant chemotherapy in breast cancer patients induces expression of miR-34a and miR-122

Transcriptional activation of cyclooxygenase-2 by tumor suppressor p53 requires nuclear factor-kappaB

Involvement of Iκbζ in glioblastomas and its potential implication in radioresistance

P‐035: RED BLOOD CELL ALLOIMMUNIZATION IN SICKLE CELL DISEASE PATIENTS IN THE DEMOCRATIC REPUBLIC OF THE CONGO

New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes

Hypogonadisme hypogonadotrope anosmique associé à une nouvelle mutation hétérozygote c.937C>T, p.His314Tyr de l’isoforme IIIb du gène FGFR1

Increased expression of receptor activator of NF‐κB ligand (RANKL), its receptor RANK and its decoy receptor osteoprotegerin in the colon of Crohn's disease patients

Mechanisms of persistent NF-kappa B activity in the bronchi of an animal model of asthma

Caractérisation clinique, neuroendocrinienne, génétique et résultats thérapeutiques dans le syndrome de Kallmann et de l’hypogonadisme normosmique idiopathique : expérience liégeoise

O9.06 PROGNOSTIC RELEVANCE AND ONCOGENIC CORRELATES OF EPILEPSY IN GLIOBLASTOMA PATIENTS

Hypogonadisme hypogonadotrope normosmique familial : identification d’une nouvelle mutation c.1664-2A > T du gène FGFR1

Étude moléculaire du gène AIP sur plus de 1400 individus atteints d’adénome hypophysaire

Une forme compliquée d’hypercalcémie hypocalciurique familiale

44P Role of DNA methylation and non-coding RNA in INK4b-ARF-INK4a locus expression

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