Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues

…, B Barret, G Firtion, N Ciraru-Vigneron, C Lacroix… - The Lancet, 1999 - thelancet.com
Background Zidovudine is commonly administered during pregnancy to prevent mother-to-child
HIV-1 transmission. We investigated mitochondrial toxic effects in children exposed to …

Persistent mitochondrial dysfunction in HIV-1-exposed but uninfected infants: clinical screening in a large prospective cohort

B Barret, M Tardieu, P Rustin, C Lacroix, B Chabrol… - Aids, 2003 - journals.lww.com
Background: Antiretroviral prevention of mother to child HIV-1 is established but tolerance
remains to be assessed. Aim: To determine the risk for persistent mitochondrial dysfunction in …

Nerve biopsy findings in different patterns of proximal diabetic neuropathy

G Said, C Goulon‐Goeau, C Lacroix… - Annals of Neurology …, 1994 - Wiley Online Library
Besides distal symmetrical sensory polyneuropathy (DSSP), middle‐aged diabetic patients
may present with focal or multifocal neuropathies, including proximal neuropathy of the lower …

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

…, C Feray, V Planté, B Ducot, P Ichai, C Lacroix… - Brain, 2000 - academic.oup.com
Familial amyloid polyneuropathy (FAP) associated with mutations of the transthyretin (TTR)
gene is the most common type of FAP, a devastating disease causing death within 10 years …

Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP)

…, A Ferreira, T Lalu, C Zaros, C Lacroix… - Neurology, 2007 - AAN Enterprises
Transthyretin familial amyloid polyneuropathies (TTR-FAPs) are autosomal dominant
neuropathies of fatal outcome within 10 years after inaugural symptoms. Late diagnosis in patients …

Nerve granulomas and vasculitis in sarcoid peripheral neuropathy: a clinicopathological study of 11 patients

G Said, C Lacroix, V Planté‐Bordeneuve, L Le Page… - Brain, 2002 - academic.oup.com
Peripheral neuropathy is a rare, yet treatable manifestation of sarcoidosis, a multisystem
disorder characterized by the presence of non‐caseating granulomas that are seldom found in …

[HTML][HTML] Hereditary Systemic Amyloidosis Due to Asp76Asn Variant β2-Microglobulin

…, P Lozeron, D Adams, C Lacroix… - … England Journal of …, 2012 - Mass Medical Soc
<p id="p005">We describe a kindred with slowly progressive gastrointestinal symptoms and
autonomic neuropathy caused by autosomal dominant, hereditary systemic amyloidosis. …

[HTML][HTML] In utero enzyme-replacement therapy for infantile-onset Pompe's disease

…, F Moretti, D Wong, C Lacroix… - … England Journal of …, 2022 - Mass Medical Soc
Patients with early-onset lysosomal storage diseases are ideal candidates for prenatal therapy
because organ damage starts in utero. We report the safety and efficacy results of in utero …

Long-term course of demyelinating neuropathies occurring during tumor necrosis factor-α–blocker therapy

P Lozeron, C Denier, C Lacroix… - Archives of Neurology, 2009 - jamanetwork.com
Objective To report the long-term follow-up (mean, 41 months; range, 25-55 months) of
patients with demyelinating neuropathy occurring after tumor necrosis factor-α (TNF-α) blocker …

Peripheral neuropathy with necrotizing vasculitis in rheumatoid arthritis

…, J Coste, C Job‐Deslandre, C Lacroix… - … : Official Journal of …, 1995 - Wiley Online Library
Objective. To examine the clinicopathologic features of the noncompressive neuropathies in
rheumatoid arthritis (RA). Methods. We studied 32 patients with RA and peripheral …