Syndrome of psychomotor retardation, bulbous nose, and epilepsy

Strong association of HLA class II sequences in Mexicans with Vogt-Koyanagi-Harada's disease.

Human immunology·1999

Predicting susceptibility of Streptococcus pneumoniae to ceftriaxone and cefotaxime by cefuroxime and ceftizoxime disk diffusion testing.

Journal of clinical microbiology·1999

Single-step PCR amplification and enzyme restriction analysis of the entire Helicobacter pylori cytotoxin vacA gene for genetic variability studies.

FEMS microbiology letters·1999

Mitochondrial DNA damage and altered membrane potential (delta psi) in pancreatic acinar cells induced by reactive oxygen species.

Surgery·1999

Establishment of experimental conditions for the rapid detection of mutations in the von Hippel-Lindau gene by parallel temperature gradient gel electrophoresis.

Electrophoresis·1999

Effects of mild protein prenatal malnutrition and subsequent postnatal nutritional rehabilitation on noradrenaline release and neuronal density in the rat occipital cortex.

Brain research. Developmental brain research·1999

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

Subtle Alterations of Tidal Breathing Variables in Healthy Late Preterm Neonates at Term-Equivalent Age.

Pediatric pulmonology·2026

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Immunological investigations·2026

Clostridium perfringens Delta toxin targets CD9 to drive NEC and brain injury.

Nature·2026

The Birth of Voice: Acoustic Baselines of Newborn Vocalizations in the First Minutes of Extrauterine Life.

Journal of voice : official journal of the Voice Foundation·2026

Optimising Paediatric Gastrostomy Outcomes Through Appropriate Procedural Selection: A 10-Year Retrospective Cohort Study.

ANZ journal of surgery·2026

EEG monitoring in the neonate as part of a multimodal brain protection system in paediatric anaesthesia.

Revista espanola de anestesiologia y reanimacion·2026

Syndrome of psychomotor retardation, bulbous nose, and epilepsy

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Strong association of HLA class II sequences in Mexicans with Vogt-Koyanagi-Harada's disease.

Predicting susceptibility of Streptococcus pneumoniae to ceftriaxone and cefotaxime by cefuroxime and ceftizoxime disk diffusion testing.

Single-step PCR amplification and enzyme restriction analysis of the entire Helicobacter pylori cytotoxin vacA gene for genetic variability studies.

Mitochondrial DNA damage and altered membrane potential (delta psi) in pancreatic acinar cells induced by reactive oxygen species.

Establishment of experimental conditions for the rapid detection of mutations in the von Hippel-Lindau gene by parallel temperature gradient gel electrophoresis.

Effects of mild protein prenatal malnutrition and subsequent postnatal nutritional rehabilitation on noradrenaline release and neuronal density in the rat occipital cortex.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

Multisite neural tube closure in humans.

Subtle Alterations of Tidal Breathing Variables in Healthy Late Preterm Neonates at Term-Equivalent Age.

Neutrophil-Derived Arg1 Impairs CD8+ T Cell Activity in Sepsis Through mTOR-Mediated Mitochondrial Dysfunction.

Clostridium perfringens Delta toxin targets CD9 to drive NEC and brain injury.

The Birth of Voice: Acoustic Baselines of Newborn Vocalizations in the First Minutes of Extrauterine Life.

Optimising Paediatric Gastrostomy Outcomes Through Appropriate Procedural Selection: A 10-Year Retrospective Cohort Study.

EEG monitoring in the neonate as part of a multimodal brain protection system in paediatric anaesthesia.

Syndrome of psychomotor retardation, bulbous nose, and epilepsy

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