[Roussy-Levi disease (Study of a familial nucleus)]

First Measurement of the Quadrupole Moment of the 2_{1}^{+} State in ^{110}Sn.

Physical review letters·2025

Abrupt structural transition in exotic molybdenum isotopes unveils an isospin-symmetric island of inversion.

Nature communications·2025

Z=14 Magicity Revealed by the Mass of the Proton Dripline Nucleus ^{22}Si.

Physical review letters·2025

Isospin Symmetry Breaking in the ^{71}Kr and ^{71}Br Mirror System.

Physical review letters·2025

First Identification of Excited States in ^{78}Zr and Implications for Isospin Nonconserving Forces in Nuclei.

Physical review letters·2025

Nuclear Structure of Dripline Nuclei Elucidated through Precision Mass Measurements of ^{23}Si, ^{26}P, ^{27,28}S, and ^{31}Ar.

Physical review letters·2024

False positive of ADA determination in cerebrospinal fluid.

Acta neurologica·1994

Post-radiation cerebral lesions in adults.

Acta neurologica·1994

A case of type I Arnold-Chiari malformation of anomalous onset.

Acta neurologica·1994

BAEP and E.M.G. changes from whiplash injuries.

Acta neurologica·1994

S.P.E.C.T., E.E.G. and M.R.I. investigations in complex partial epilepsy.

Acta neurologica·1994

Early cognitive impairment in multiple sclerosis detected by a screening with a vocabulary-test.

Acta neurologica·1994

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

[Roussy-Levi disease (Study of a familial nucleus)]

Related Concept Videos

First Measurement of the Quadrupole Moment of the 2_{1}^{+} State in ^{110}Sn.

Abrupt structural transition in exotic molybdenum isotopes unveils an isospin-symmetric island of inversion.

Z=14 Magicity Revealed by the Mass of the Proton Dripline Nucleus ^{22}Si.

Isospin Symmetry Breaking in the ^{71}Kr and ^{71}Br Mirror System.

First Identification of Excited States in ^{78}Zr and Implications for Isospin Nonconserving Forces in Nuclei.

Nuclear Structure of Dripline Nuclei Elucidated through Precision Mass Measurements of ^{23}Si, ^{26}P, ^{27,28}S, and ^{31}Ar.

False positive of ADA determination in cerebrospinal fluid.

Post-radiation cerebral lesions in adults.

A case of type I Arnold-Chiari malformation of anomalous onset.

BAEP and E.M.G. changes from whiplash injuries.

S.P.E.C.T., E.E.G. and M.R.I. investigations in complex partial epilepsy.

Early cognitive impairment in multiple sclerosis detected by a screening with a vocabulary-test.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

[Roussy-Levi disease (Study of a familial nucleus)]

Related Concept Videos

Related Articles