Image de couverture de livre

Differential Test of the Internal Structure of the Electron through the Bound g Factor

Fuente: Zenodo

Enregistré dans:

Détails bibliographiques
Auteur principal:	Zamboni, Lino
Format:	Recurso digital
Langue:	anglais
Publié:	Zenodo 2026
Sujets:	Structured Electron , Magnetic Anomaly , Bound g Factor , Hydrogenlike and Lithiumlike ions , Electromagnetic internal Response
Accès en ligne:	Acceder al recurso
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires

Proof of the Existence of "Magnetic" and Interpretation of Space Proposed in Magnetic Space Cosmology
par: Kim, H.S
Publié: (2025)

[Paper 7] The Holographic Time Principle: Lorentz Symmetry, Arrow of Time, and Equivalence from 4-Bit Unitarity
par: Nguyen, Khoa
Publié: (2026)

Improvement of speech function in submucous cleft palate through conservative treatment
par: Nagana Natsume, et autres
Publié: (2025)

INCIDENT RESPONSE AUTOMATION
par: ijesat
Publié: (2026)

The Field Potential W: A Constructive Foundation for Classical Electromagnetism
par: Olawale, Akintunde Abiodun
Publié: (2026)

GPS Total Electron Content measurements at low latitudes in Brazil for low solar activity
par: J. Williams Vilas Boas
Publié: (2004)

A Complete Proof for the Derivation of the Fine-Structure Constant from Prime Number Dynamics.
par: Okolo, Hanyelichukwu Paul
Publié: (2025)

A Case of HNRNPU ‐Related Neurodevelopmental Disorder Presenting With Acute Encephalopathy and Basal Ganglia Lesions
par: Syunsuke Nagara, et autres
Publié: (2026)

Severe pharyngeal stenosis and laryngomalacia in an individual of HNRNPU ‐related neurodevelopmental disorder associated with a novel nonsense variant
par: Yusuke Sasaki, et autres
Publié: (2025)

Non‐Immune Hydrops Fetalis, Multifocal Chorangiomatosis, and Noonan Syndrome 8
par: Eugen‐Matthias Strehle, et autres
Publié: (2025)

Assisted reproduction and congenital malformations: A systematic review and meta‐analysis
par: Meenakshi Veeramani, et autres
Publié: (2024)

Morphogenesis of the Extraocular Muscles During the Human Embryonic and Early Fetal Periods
par: Miho Osaka, et autres
Publié: (2026)

A case series study on the safety of cefditoren pivoxil use during the first trimester of pregnancy in Japan
par: Mariko Honma, et autres
Publié: (2024)

Acoustic evaluation of voice signal distortion by videoconferencing platforms and devices used in telepractice for cleft palate
par: Shiho Tajiri, et autres
Publié: (2024)

Questionnaire survey on public awareness of cleft lip with/without palate in Mongolia
par: Anar‐Erdene Gantugs, et autres
Publié: (2024)

Postnatal Bimodal Dynamics and Androgen‐Induced Masculinization of the External Genitalia in Mice
par: Junki Aikawa, et autres
Publié: (2026)

Urinary Metabolic Screening Misled the Molecular Diagnosis of Xia–Gibbs Syndrome
par: Sayaka Enomoto, et autres
Publié: (2026)

Risk of major birth defects after first‐trimester exposure to carbocisteine and ambroxol: A multicenter prospective cohort study using counseling data for drug safety during pregnancy
par: Mariko Usuda, et autres
Publié: (2024)

Morphological relationship between the cranial base and facial anomalies in humans: Challenges and future perspectives
par: Natsuko Utsunomiya, et autres
Publié: (2025)

Predictability of fetal pulmonary artery Doppler on neonatal outcomes in pregnant women with gestational diabetes mellitus
par: Huriye Ezveci, et autres
Publié: (2025)

Compound heterozygous ZNF335 variants in a patient with microcephaly, refractory epilepsy, and severe developmental delay: A case report and literature review
par: Kaori Yamoto, et autres
Publié: (2025)

Risk factors for isolated congenital heart defects in infants from Western Mexico
par: Jessica Paola Cruz‐Cruz, et autres
Publié: (2024)

Pyramidalis muscle formation during human embryonic and early fetal periods
par: Yui Iwasa, et autres
Publié: (2024)

Co‐Occurrence of Urogenital Anomalies and Congenital Heart Disease in a Child With Alpha‐Thalassemia Mental Retardation Syndrome Associated With Chromosome 16 Abnormalities due to Partial Monosomy 16p13.3 and Partial Trisomy 16q22.1–q24.3
par: Hideki Tamaru, et autres
Publié: (2025)

Focused Clinical Observation of Functional Outcomes in Children With OEIS Complex
par: Osamu Yazawa, et autres
Publié: (2026)

A cohort study on structural analysis of congenital anomalies in an intensive care unit in Azerbaijan
par: Narmin Akif Azizova, et autres
Publié: (2025)

Patients With Hereditary Hemorrhagic Telangiectasia Diagnosed by Nanopore Long Read Sequencer
par: Mamiko Yamada, et autres
Publié: (2025)

Cervical vertebrae fusion in elbow knee synostosis ( Eks )‐mutant mice with fibroblast growth factor 9 N143T mutation
par: Georgina Djameh, et autres
Publié: (2025)

Revisiting ultrasonographic soft markers of aneuploidy: A thoughtful analysis in low‐risk and screening naïve Indian antenatal women
par: Shreya Das, et autres
Publié: (2025)

Correction to “Cohort Study of Pregnancy Outcomes After Exposure to Fexofenadine or Olopatadine in the First Trimester”
Publié: (2026)

A C ‐Propeptide Variant in COL1A1 Potentially Perturbing Disulfide Bonding in Osteogenesis Imperfecta Type III
par: Daisuke Watanabe, et autres
Publié: (2026)

Correction to: “Patterns of Primary and Secondary Defects Associated With Non‐Syndromic Cleft Lip and Palate: An Epidemiological Analysis in a Kenyan Population”
Publié: (2025)

Congenital cardiac anomalies in non‐syndromic cleft lip and cleft palate patients: A systematic review and meta‐analysis
par: Bindey Kumar, et autres
Publié: (2024)

Cohort Study of Pregnancy Outcomes After Exposure to Fexofenadine or Olopatadine in the First Trimester
par: Kaori Yamazaki, et autres
Publié: (2026)

Upper airway obstruction due to congenital epiglottic cyst: Report of two cases
par: Kensuke Uraguchi, et autres
Publié: (2024)

The Japanese Teratology Society 65th Annual Meeting July 25–27, 2025
Publié: (2025)

Refractory congenital chylous ascites—Case report of a successful surgical management
par: Inês Araújo Oliveira, et autres
Publié: (2025)

The role of sonic hedgehog signaling in the oropharyngeal epithelium during jaw development
par: Rika Takeuchi, et autres
Publié: (2024)

Accumulation of ether phospholipids in induced pluripotent stem cells and oligodendrocyte‐lineage cells established from patients with Sjögren‐Larsson syndrome
par: Yu Yamaguchi, et autres
Publié: (2024)

Refining the Neonatal Phenotypic Spectrum of Distal Deletion 14q Syndrome: Early Genomic Diagnosis in Infancy
par: Koji Nakae, et autres
Publié: (2026)