470 results on '"Yahyaoui M"'
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2. Investigation of type-II Ga(As)Sb/GaAs quantum dots embedded in an InGaAs quantum well for solar cell applications
3. Syndrome de moyamoya et lupus
4. Corrigendum to “Electrical and dielectric properties of ferromagnetic GeMn nanocrystals embedded in metal-oxide-semiconductor Schottky diodes (Al/SiO2:GeMn NCs/n-Si) grown by MBE” [Vacuum 224 (2024) 113191]
5. Theoretical and experimental investigation of nano-materials based on Ge–Mn for third-generation solar cells
6. PHYTOCHEMICAL COMPOSITION, ANTIBACTERIAL EFFICACY, AND SYNERGISTIC INTERACTIONS OF CLINOPODIUM NEPETA SUBS ASCENDENS ESSENTIAL OIL IN COMBINATION WITH CONVENTIONAL ANTIBIOTICS.
7. Segregation of the InDel Mutation in IRF2BP2 Discriminating Fleece Type in North African and Iranian Sheep Breeds.
8. Poliomyelitis alert on Tunisian borders: response and challenges
9. Neutral, charged excitons and biexcitons in strain-free and asymmetric GaAs quantum dots fabricated by local droplet etching
10. Stroke and syphilis: A retrospective study of 53 patients
11. Association of vitamin D status with multiple sclerosis in a case-control study from Morocco
12. Vitamin D deficiency and its role in neurological conditions: A review
13. Evaluation of retinal nerve fiber layer thickness measured by optical coherence tomography in Moroccan patients with multiple sclerosis
14. A clinical study of non-parkinsonian tremor in Moroccan patients
15. Profile of multiple system atrophy in Moroccan patients attending a movement disorders outpatient clinic in Rabat university hospital
16. Qualité de vie et sclérose en plaques : traduction en langue arabe et adaptation transculturelle du « MSQOL-54 »
17. Neurological manifestations of Behçet's disease: Evaluation of 40 patients treated by cyclophosphamide
18. Trouble psychotique révélant une épilepsie associée à une tumeur dysembryoplasique neuroépithétliale de l’hippocampe gauche
19. Pneumopathie interstitielle et artérite à cellules géantes : bien plus que le Horton tussigène !
20. Efficacité et tolérance du cyclophosphamide dans le traitement de fond des formes progressives de la sclérose en plaques
21. La maladie de Vogt-Koyanagi-Harada : plaidoyer pour un traitement intensif
22. Neuropathie optique ischémique antérieure aiguë artéritique avec CRP négative, ne pas se laisser tromper par les facteurs de risque vasculaire !
23. Experimental and modelling study of gasoline surrogate mixtures oxidation in jet stirred reactor and shock tube
24. The effect of strain and indium content on the optical properties of GaInAs/GaAs ternary alloys
25. Excitonic complexes in strain-free and highly symmetric GaAs quantum dots fabricated by filling of self-assembled nanoholes.
26. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients
27. Neurological Manifestations in Behcet Disease
28. Pseudo-aïnhum et neuropathie axonale
29. Temperature-dependent transport properties of CVD-fabricated n-GaN nanorods/p-Si heterojunction devices
30. Rituximab et néphropathie lupique
31. Le neuro-Behçet parenchymateux
32. Manifestations cardiaques au cours de la granulomatose éosinophilique avec polyangéite
33. Le TAFRO syndrome : une nouvelle sous-entité de la maladie de Castleman
34. La mucormycose orbito-facial et pulmonaire mimant une granulomatose avec polyangéite
35. Transformation maligne et syndrome de Gougerot-Sjögren
36. Experimental and modeling study of 1-hexene oxidation behind reflected shock waves
37. Optical properties of LiNbO3 crystals doped with Yb3+ ions.
38. CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY (CIDP): A STUDY OF 37 CASES
39. Evaluation of the impact of wastewater in the rural commune of Jmaa Moulblad on the bacteriological water quality of the Grou River (Rabat region, Morocco)
40. Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia
41. Hypertension intracrânienne bénigne: Aspects cliniques et thérapeutiques
42. Behçetʼs disease in Moroccan children: a report of 12 cases
43. Phenotypical features of 12 Moroccan families with autosomal recessive Charcot-Marie-Tooth disease associated with mutations in GDAP1 gene: SC315
44. Mapping of the goat stearoyl coenzyme A desaturase gene to chromosome 26
45. Inferring the population structure of the Maghreb sheep breeds using a medium‐density SNP chip
46. Sarcoidose multisystémique révélée par une hypersomnolence
47. Atrophie cérébelleuse révélant une association entre la thyroïdite d’Hashimoto et le syndrome de Gougerot–Sjogren
48. Mentha pulegium : une cause rare du syndrome de vasoconstriction cérébrale réversible (SVCR)
49. Délabrement traumatique de la face dorsale du médiopied. À propos d’un cas
50. La maladie de Wilson. Étude clinique, thérapeutique et évolutive de 21 cas
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