D. Adams

V. Algalarrondo, D. Adams, T. Antonini, 2014, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation

C. Lacroix, P. Lozeron, M. Gugenheim, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Long-term course of demyelinating neuropathies occurring during tumor necrosis factor-alpha-blocker therapy.

C. Lacroix, P. Lozeron, D. Adams, 2009, Archives of neurology.

Long-term Course of Demyelinating Neuropathies Occurring During Tumor Necrosis Factor-– Blocker Therapy

C. Lacroix, P. Lozeron, D. Adams, 2009 .

Motor neuron syndromes and monoclonal IgM antibodies to gangliosides.

A. Steck, D. Adams, 1991, Advances in neurology.

Monoclonal gammopathy and neuropathy

P. Lozeron, D. Adams, 2007, Current opinion in neurology.

Acute myeloradiculitis duetocytomegalovirus asthe initial manifestation ofAIDS

R. Gherardi, D. Adams, F. Mahieux, 1989 .

Immunological Hallmarks of JC Virus Replication in Multiple Sclerosis Patients on Long-Term Natalizumab Therapy

C. Louapre, B. Stankoff, C. Giannesini, 2013, Journal of Virology.

Advances in the treatment of chronic inflammatory demyelinating neuropathies in 2010

P. Lozeron, D. Adams, 2011, Journal of Neurology.

Varicella-zoster virus acute myelitis in a patient with MS treated with natalizumab

D. Adams, M. Théaudin, C. Cauquil, 2013, Neurology.

Hereditary and acquired amyloid neuropathies

D. Adams, 2001, Journal of Neurology.

FAP Neuropathy and Emerging Treatments

V. Algalarrondo, M. Slama, D. Adams, 2014, Current Neurology and Neuroscience Reports.

Amyloid neuropathies.

C. Lacroix, P. Lozeron, D. Adams, 2012, Current opinion in neurology.

The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation.

S. Metral, C. Lacroix, D. Samuel, 2000, Brain : a journal of neurology.

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy

D. Booth, A. Harding, P. Thomas, 1996, Neuromuscular Disorders.

Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses

P. Latour, S. Attarian, D. Adams, 2016, Journal of Neurology, Neurosurgery & Psychiatry.

Contribution of nerve biopsy findings to the diagnosis of disabling neuropathy in the elderly. A retrospective review of 100 consecutive patients.

C. Lacroix, D. Adams, G. Said, 1996, Brain : a journal of neurology.

From immunosuppression to tolerance.

D. Samuel, A. Sánchez‐Fueyo, D. Adams, 2015, Journal of hepatology.

Phase 2 Open-Label Extension Study (OLE) of Patisiran, an Investigational RNAi Therapeutic for Familial Amyloid Polyneuropathy (FAP) (S38.003)

B. Bettencourt, K. Gruis, J. Gollob, 2016 .

MRI for the detection of Restrictive Cardiomyopathy in Familial Amyloid Polyneuropathy

V. Algalarrondo, D. Adams, S. Dinanian, 2005 .

[Multifocal motor neuropathies with conduction blocks. 39 cases].

V. Meininger, N. Baumann, N. Birouk, 1997, Revue neurologique.

JC virus granule cell neuronopathy and hyper-IgE in HIV disease

D. Adams, T. Shang, A. Delgado, 2011, Neurology.

Late‐onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France

D. Adams, G. Said, G. Grateau, 1993, Clinical genetics.

Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)

A. Harding, M. Davis, M. Reilly, 1995, Journal of Neurology.

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy.

D. Booth, A. Harding, P. Thomas, 1995 .

First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy

B. Hazenberg, E. Hund, M. Slama, 2016, Current opinion in neurology.

Somatostatin analogues for refractory diarrhoea in familial amyloid polyneuropathy

F. Carbonnel, D. Adams, G. Antoni, 2018, PloS one.

IDENTIFICATION OF TRANSTHYRETIN FAMILIAL AMYLOID POLYNEUROPATHY IN NEW COUNTRIES

D. Adams, C. Cauquil, C. Labeyrie, 2017 .

Phase 1 study of ALN-TTRsc02, a subcutaneously administered investigational RNAi therapeutic for the treatment of transthyretin-mediated amyloidosis

D. Adams, Karsten Verena, 2019, Revue Neurologique.

Neuropathies motrices multifocales avec blocs de conduction: 39 cas

V. Meininger, N. Baumann, N. Birouk, 1997 .

Transthyretin amyloid polyneuropathies mimicking a demyelinating polyneuropathy

P. Lozeron, B. Arnulf, D. Adams, 2018, Neurology.

Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease

M. Slama, D. Adams, T. Coelho, 2019, Nature Reviews Neurology.

Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy

P. Hawkins, M. Gertz, G. Merlini, 2020, Journal of Neurology.

Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP

David Adams, Teresa Coelho, Y. Parman, 2016, Current opinion in neurology.

[New elements in the diagnosis and the treatment of primary AL amyloid polyneuropathy and neuropathy due to POEMS syndrome].

J. Bourhis, C. Lacroix, P. Lozeron, 2011, Revue neurologique.

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

K. Bhatia, A. Harding, P. Thomas, 1993, Journal of neurology, neurosurgery, and psychiatry.

French patients with amyloid neuropathy . Transthyretin gene mutations in British and

A. Harding, P. Thomas, M. Davis, 2022 .

Multifocal deficits due to leukemic meningoradiculitis in chronic lymphocytic leukemia

C. Lacroix, P. Lozeron, V. Ribrag, 2009, Journal of the Neurological Sciences.

Inflammatory demyelinating polyneuropathies and lymphoma: clues to diagnosis and therapy

O. Lambotte, C. Goujard, D. Adams, 2021, Leukemia & lymphoma.

Acquired and inherited amyloidosis: Knowledge driving patients' care

D. Adams, L. Obici, 2020, Journal of the peripheral nervous system : JPNS.

[Cervical spinal sarcoidosis mimicking compressive cervical myelopathy: Poor prognosis after surgery].

O. Lambotte, C. Goujard, D. Adams, 2019, La Revue de medecine interne.

Myocardial Muscarinic Receptor Upregulation and Normal Response to Isoproterenol in Denervated Hearts by Familial Amyloid Polyneuropathy

P. Merlet, J. Delforge, D. Samuel, 2001, Circulation.

Symptomatic and proven de novo amyloid polyneuropathy in familial amyloid polyneuropathy domino liver recipients

C. Lacroix, D. Samuel, P. Lozeron, 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Inflammatory vasculopathy in multifocal diabetic neuropathy.

C. Lacroix, P. Lozeron, D. Adams, 2003, Brain : a journal of neurology.

Vasculitis neuropathy mimicking lower limb mono-radiculopathy: a study and follow-up of 8 cases

C. Lacroix, P. Lozeron, D. Adams, 2013, Internal and Emergency Medicine.

Reversibility of Acquired Amyloid Polyneuropathy After Liver Retransplantation

C. Lacroix, D. Samuel, P. Lozeron, 2013, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Impact of Liver Transplantation on Cardiac Autonomic Denervation in Familial Amyloid Polyneuropathy

P. Merlet, D. Samuel, D. Le Guludec, 2006, Medicine.

Changes in renal function in patients with familial amyloid polyneuropathy treated with orthotopic liver transplantation.

D. Samuel, P. Bedossa, H. Bismuth, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Cardiac denervation evidenced by MIBG occurs earlier than amyloid deposits detection by diphosphonate scintigraphy in TTR mutation carriers

D. Le Guludec, F. Rouzet, V. Algalarrondo, 2018, European Journal of Nuclear Medicine and Molecular Imaging.

Cardiac sympathetic denervation in familial amyloid polyneuropathy assessed by iodine-123 metaiodobenzylguanidine scintigraphy and heart rate variability

P. Merlet, D. Samuel, D. Le Guludec, 1999, European Journal of Nuclear Medicine.

Painful proximal diabetic neuropathy: Inflammatory nerve lesions and spontaneous favorable outcome

C. Lacroix, D. Adams, G. Said, 1997, Annals of neurology.

Spectrum and prognosis of neurologic complications after hematopoietic transplantation

C. Lacroix, S. Koscielny, J. Bosq, 2006, Neurology.

Conjunctival lymphangiectasia: a novel ocular manifestation of hereditary transthyretin amyloidosis

M. Labetoulle, E. Barreau, A. Rousseau, 2019, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case report

C. Lacroix, L. Mouthon, A. Brézin, 2017, Journal of Medical Case Reports.

Potential Role of In Vivo Confocal Microscopy for Imaging Corneal Nerves in Transthyretin Familial Amyloid Polyneuropathy.

David Adams, Christophe Baudouin, Marc Labetoulle, 2016, JAMA ophthalmology.

Small fiber neuropathy in Sjögren syndrome: Comparison with other small fiber neuropathies

X. Mariette, R. Seror, D. Adams, 2020, Muscle & nerve.

Gadolinium-enhanced MRI in central nervous system Behçet's disease

R. Carlier, P. Masnou, D. Adams, 2004, Neuroradiology.

Clinicopathologic findings and prognosis of chronic inflammatory demyelinating polyneuropathy

F. Chédru, C. Lacroix, C. Bouchard, 1999, Neurology.

Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis

S. Ajroud‐Driss, M. Sweetser, H. Schmidt, 2020, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Brentuximab vedotin treatment associated with acute and chronic inflammatory demyelinating polyradiculoneuropathies

T. Maisonobe, A. Echaniz-Laguna, Adrien Wang, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Comparison of Lewis–Sumner syndrome with chronic inflammatory demyelinating polyradiculoneuropathy patients in a tertiary care centre

T. Maisonobe, D. Adams, C. Labeyrie, 2020, European journal of neurology.

Diagnostic usefulness of plexus magnetic resonance imaging in chronic inflammatory demyelinating polyradiculopathy without electrodiagnostic criteria of demyelination

D. Adams, M. Théaudin, C. Labeyrie, 2018, European journal of neurology.

Specific postoperative complications of vitrectomy in hereditary transthyretin amyloidosis

M. Labetoulle, E. Barreau, A. Rousseau, 2021, European journal of ophthalmology.

When to suspect transthyretin amyloidosis in cases of isolated vitreous opacities?

M. Labetoulle, E. Barreau, A. Rousseau, 2020, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Multifocal neuropathy due to plasma cell infiltration of peripheral nerves in multiple myeloma

C. Lacroix, P. Lozeron, D. Decaudin, 2006, Neurology.

Ultrastructural characterisation of the M protein in nerve biopsy of patients with POEMS syndrome

D. Adams, G. Said, 1998, Journal of neurology, neurosurgery, and psychiatry.

Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose study

B. Bettencourt, J. Gollob, H. Schmidt, 2015, Orphanet Journal of Rare Diseases.

Contribution of plexus MRI in the diagnosis of atypical chronic inflammatory demyelinating polyneuropathies

C. Lacroix, P. Lozeron, D. Adams, 2016, Journal of the Neurological Sciences.

Intracerebral Hemorrhage Caused by Thrombosis of Developmental Venous Anomaly: Total Recovery following Anticoagulation

D. Ducreux, D. Adams, C. Denier, 2010, European Neurology.

Varied patterns of inaugural light-chain (AL) amyloid polyneuropathy: a monocentric study of 24 patients

C. Lacroix, P. Lozeron, P. Corcia, 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver Transplantation.

D. Chemla, C. Lacroix, D. Samuel, 2016, JACC. Cardiovascular imaging.

Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathy

D. Chemla, D. Samuel, D. Le Guludec, 2018, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

ALN-TTR, an RNAI therapeutic for the treatment of transthyretin amyloidosis

P. Lozeron, L. Nechev, P. Hawkins, 2011 .

A brief compound test for assessment of autonomic and sensory-motor dysfunction in familial amyloid polyneuropathy

P. Lozeron, V. Planté-Bordeneuve, D. Adams, 2007, Journal of Neurology.

Safety of intravenous immunoglobulin in the elderly treated for a dysimmune neuromuscular disease

P. Lozeron, P. Masnou, D. Adams, 2015, Muscle and Nerve.

Conjunctival lymphangiectasia as a biomarker of severe systemic disease in Ser77Tyr hereditary transthyretin amyloidosis

M. Labetoulle, V. Algalarrondo, M. Slama, 2020, British Journal of Ophthalmology.

Abstracts from the First European Meeting for ATTR Amyloidosis for Doctors and Patients

M. Sweetser, J. Gollob, I. Conceição, 2017, Orphanet Journal of Rare Diseases.

A small deep infarct revealing leukoencephalopathy, calcifications and cysts in an adult patient

D. Adams, C. Denier, I. Wargon, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.