Results 21 to 30 of about 157,606 (247)
Time to AIDS from 1992 to 1999 in HIV-1-Infected Subjects with Known Date of Infection. [PDF]
To estimate the change in AIDS incubation time during three periods characterized by different availability of antiretroviral treatments, data from the French Hospital Database on HIV of 4702 HIV-1-positive subjects with a documented date of infection ...
Bentata, M +5 more
core +2 more sources
Acute Inflammatory Demyelination: MRI Prognostic Factors for Relapse
Initial MRI factors predictive of a second attack and disability following a first episode of acute CNS inflammatory demyelination in a cohort of 116 children seen between 1990 and 2002 were studied at the Hopital Cochin-Saint-Vincent de Paul, Paris ...
J Gordon Millichap
doaj +1 more source
Severe congenital microcephaly with AP4M1 mutation, a case report [PDF]
Background: Autosomal recessive defects of either the B1, E1, M1 or S1 subunit of the Adaptor Protein complex-4 (AP4) are characterized by developmental delay, severe intellectual disability, spasticity, and occasionally mild to moderate microcephaly of ...
Abramowicz, Marc +6 more
core +2 more sources
Adaptive mitochondrial mechanisms allow mitochondrial resilience and prevent the worsening of fibrosis, while deregulation of these mechanisms promotes the progression from no/minimal‐mild (F0‐F2) fibrosis to advanced fibrosis and cirrhosis (F3‐F4). Abstract Background and Aims Hepatitis B virus (HBV) infection causes oxidative stress (OS) and alters ...
Dimitri Loureiro +17 more
wiley +1 more source
Peripheral Neuropathy and Hereditary Tyrosinemia
Neurologic crises in 48 children with tyrosinemia identified on neonatal screening since 1970 are described from the Departments of Genetics, Hopital Sainte Justine, Hopital de Chicoutimi; and Universite Laval, Quebec, Canada.
J Gordon Millichap
doaj +1 more source
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source
RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease
RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease. Abstract Background and Aims Receptor‐interacting protein kinase 3 (RIPK3) mediates NAFLD progression, but its metabolic function is unclear. Here, we aimed to investigate the role of RIPK3 in modulating mitochondria function, coupled with lipid droplet (LD)
Marta B. Afonso +16 more
wiley +1 more source
Acute Encephalopathy of Obscure Origin
Six previously healthy children who developed an acute encephalopathy several days after a prodromal illness are reported from the Hopital Bicetre, and Hopital Necker-Enfants Malades, Paris, France.
J Gordon Millichap
doaj +1 more source
Discrètement licencieuses ou franchement pornographiques, les fresques des salles de garde des Internes en médecine intriguent, amusent, fascinent. De nombreux « beaux livres » et de savantes études ethnologiques leur ont été consacrés.
Christian Hottin
doaj +1 more source
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development [PDF]
Bosma arhinia microphthalmia syndrome (BAMS) is an extremely rare and striking condition characterized by complete absence of the nose with or without ocular defects.
A Javed +97 more
core +3 more sources

