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Amenagement urbain et organisations populaires : le cas des quartiers de Belem do Para (Bresil)

Serre, Agnes

2000

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Patrimoine et politique d’aménagement : du fonctionnalisme à l’émergence d’une culture urbaine à Belém do Pará (Brésil)

Géocarrefour : revue de géographie de Lyon, 2004-07, Vol.79 (3), p.239-246

Serre, Agnès

2004

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Patrimoine et politique d'aména gement : du fonctionalisme à l'émergence d'une culture urbaine à belém do paré (Brésil): Patrimoine et aménagement urbain

Géocarrefour : revue de géographie de Lyon, 2004, Vol.79 (3), p.239-246

SERRE, Agnès

2004

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Construction d'une identité urbaine par l'utilisation d'imagerie. Le cas de Benguí, favela d'Amazonie brésilienne

Autrepart, 2002-12, Vol.24 (4), p.69-87

Serre, Agnès

2002

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Patrimoine et aménagement urbain

Géocarrefour : revue de géographie de Lyon, 2004, Vol.79 (3)

2004

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Belém, une ville amazonienne. Aménagement du territoire et organisations populaires

Lusotopie, 2002, Vol.1 (10), p.249-250

2002

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Mutation of RRM2B , encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

Nature genetics, 2007-06, Vol.39 (6), p.776-780

2007

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CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

American journal of human genetics, 2008-03, Vol.82 (3), p.623-630

2008

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Common bean resistance to Xanthomonas is associated with upregulation of the salicylic acid pathway and downregulation of photosynthesis

BMC genomics, 2020-08, Vol.21 (1), p.566-566, Article 566

2020

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Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy

American journal of human genetics, 2017-01, Vol.100 (1), p.151-159

2017

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Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy

Human mutation, 2011-11, Vol.32 (11), p.1225-1231

2011

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Mutation in PNPT1, which Encodes a Polyribonucleotide Nucleotidyltransferase, Impairs RNA Import into Mitochondria and Causes Respiratory-Chain Deficiency

American journal of human genetics, 2012-11, Vol.91 (5), p.912-918

2012

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Impaired Transferrin Receptor Palmitoylation and Recycling in Neurodegeneration with Brain Iron Accumulation

American journal of human genetics, 2018-02, Vol.102 (2), p.266-277

2018

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Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

Journal of thrombosis and haemostasis, 2021-08, Vol.19 (8), p.1959-1972

2021

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Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy

Journal of medical genetics, 2017-05, Vol.54 (5), p.346-356

2017

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Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency

Biochimica et biophysica acta, 2013-08, Vol.1832 (8), p.1304-1312

2013

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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Neurobiology of aging, 2014-12, Vol.35 (12), p.2884.e1-2884.e4

2014

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Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion

Annals of neurology, 2007-12, Vol.62 (6), p.579-587

2007

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Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles

BMC medical genetics, 2009-06, Vol.10 (51), p.51-51, Article 51

2009

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TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy

American journal of human genetics, 2009-04, Vol.84 (4), p.493-498

2009

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Induction Therapy in Elderly Kidney Transplant Recipients With Low Immunological Risk

Transplantation, 2020-03, Vol.104 (3), p.613-622

2020

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Standard-dose versus higher-dose prophylactic cranial irradiation (PCI) in patients with limited-stage small-cell lung cancer in complete remission after chemotherapy and thoracic radiotherapy (PCI 99-01, EORTC 22003-08004, RTOG 0212, and IFCT 99-01): a randomised clinical trial

The lancet oncology, 2009-05, Vol.10 (5), p.467-474

2009

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Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Brain (London, England : 1878), 2011, Vol.134 (Pt 1), p.210-219

2011

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Dynamic predictions of long-term kidney graft failure: an information tool promoting patient-centred care

Nephrology, dialysis, transplantation, 2019-11, Vol.34 (11), p.1961-1969

2019

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Impact of puberty as threshold to differentiate outcome of out-of-hospital cardiac arrest care groups: a nationwide observational study in France

Emergency medicine journal : EMJ, 2022-05, Vol.39 (5), p.363-369

2022

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Amenagement urbain et organisations populaires : le cas des quartiers de Belem do Para (Bresil)

Patrimoine et politique d’aménagement : du fonctionnalisme à l’émergence d’une culture urbaine à Belém do Pará (Brésil)

Patrimoine et politique d'aména gement : du fonctionalisme à l'émergence d'une culture urbaine à belém do paré (Brésil): Patrimoine et aménagement urbain

Construction d'une identité urbaine par l'utilisation d'imagerie. Le cas de Benguí, favela d'Amazonie brésilienne

Patrimoine et aménagement urbain

Belém, une ville amazonienne. Aménagement du territoire et organisations populaires

Mutation of RRM2B , encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

Common bean resistance to Xanthomonas is associated with upregulation of the salicylic acid pathway and downregulation of photosynthesis

Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy

Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy

Mutation in PNPT1, which Encodes a Polyribonucleotide Nucleotidyltransferase, Impairs RNA Import into Mitochondria and Causes Respiratory-Chain Deficiency

Impaired Transferrin Receptor Palmitoylation and Recycling in Neurodegeneration with Brain Iron Accumulation

Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy

Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency

Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion

Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles

TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy

Induction Therapy in Elderly Kidney Transplant Recipients With Low Immunological Risk

Standard-dose versus higher-dose prophylactic cranial irradiation (PCI) in patients with limited-stage small-cell lung cancer in complete remission after chemotherapy and thoracic radiotherapy (PCI 99-01, EORTC 22003-08004, RTOG 0212, and IFCT 99-01): a randomised clinical trial

Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Dynamic predictions of long-term kidney graft failure: an information tool promoting patient-centred care

Impact of puberty as threshold to differentiate outcome of out-of-hospital cardiac arrest care groups: a nationwide observational study in France

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