205 results on '"Neri, Giovanni"'
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2. Cover Feature: Voltammetric Sensor Based on Waste‐Derived Carbon Nanodots for Enhanced Detection of Nitrobenzene (ChemElectroChem 13/2023)
3. Voltammetric Sensor Based on Waste‐Derived Carbon Nanodots for Enhanced Detection of Nitrobenzene
4. Dermatological manifestations, management, and care in RASopathies
5. Molecular advances, clinical management, and treatment opportunities in RASopathies
6. Development of a novel electrochemical nitrite sensor based on Zn‐Schiff base complexes
7. Syndromes and birth defects in art and antiquities: New perspectives on a familiar theme
8. The earliest depictions of a PIK3CA‐Related Overgrowth Spectrum disorder: 17th‐18th century prints of women with severe limb overgrowth
9. Overgrowth in myth and art
10. Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma
11. CARDIO‐FACIO‐CUTANEOUS SYNDROME
12. Unilateral unifocal advanced intraocular retinoblastoma: is reasonable to adopt intra‐arterial chemotherapy as single therapeutic choice?
13. X‐linked intellectual disability: Phenotypic expression in carrier females
14. Gas Sensing of NiO‐SCCNT Core–Shell Heterostructures: Optimization by Radial Modulation of the Hole‐Accumulation Layer
15. Preliminary experience of the use of high-resolution skin ultrasound for the evaluation of extrathyroidal manifestations of Graves’ disease and response to UVA-1 phototherapy
16. Tuning the NiO Thin Film Morphology on Carbon Nanotubes by Atomic Layer Deposition for Enzyme‐Free Glucose Sensing
17. X-linked intellectual disability update 2017
18. Non-enzymatic Glucose Sensor Based on Nickel/Carbon Composite
19. “Minimal” holoprosencephaly in a 14q deletion syndrome patient
20. Variations on the theme of how to write a scientific article
21. CD93 as a Potential Target in Neovascular Age‐Related Macular Degeneration
22. Simpson-Golabi-Behmel syndrome in a female: A case report and an unsolved issue
23. Recognizable facial features in patients with alternating hemiplegia of childhood
24. Nanostructured Materials for Room‐Temperature Gas Sensors
25. Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes
26. Electrochemical Properties of Ag@iron Oxide Nanocomposite for Application as Nitrate Sensor
27. The intellectual disabilities evaluation and advice system (IDEAS): Outcome of the first 55 cases
28. The perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
29. Historical perspective on developmental concepts and terminology
30. Epilepsy in ring 14 syndrome: A clinical and EEG study of 22 patients
31. Amperometric Sensing of H2O2using Pt-TiO2/Reduced Graphene Oxide Nanocomposites
32. Room-Temperature Hydrogen Sensing with Heteronanostructures Based on Reduced Graphene Oxide and Tin Oxide
33. Three unrelated patients with congenital anterior pituitary aplasia and a characteristic physical and neuropsychological phenotype: A new syndrome?
34. Chromosome 9p deletion syndrome and sex reversal: Novel findings and redefinition of the critically deleted regions
35. Simpson–Golabi–Behmel syndrome type 1 in a 27‐week macrosomic preterm newborn: The diagnostic value of rib malformations and index nail and finger hypoplasia
36. Photoreduction of Mesoporous In2O3: Mechanistic Model and Utility in Gas Sensing
37. Autism and intellectual disability: Two sides of the same coin
38. Expanding the spectrum of rearrangements involving chromosome 19: A mild phenotype associated with a 19p13.12–p13.13 deletion
39. The FRAXopathies: Definition, overview, and update
40. ChemInform Abstract: Metal Oxide Nanostructures for Solid State Gas Sensors: A Recent Patent Survey
41. Tin Dioxide Sensing Layer Grown on Tubular Nanostructures by a Non-Aqueous Atomic Layer Deposition Process
42. Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome
43. Response to “Valproic Acid and ADHD Symptoms in Fragile X Syndrome: More Evidence Is Needed”
44. Unexpected finding of a paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother
45. Treatment with valproic acid ameliorates ADHD symptoms in fragile X syndrome boys
46. Phenotypic map in ring 14 syndrome
47. Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back
48. Down syndrome: Comments and reflections on the 50th anniversary of Lejeune's discovery
49. Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome
50. Further evidence that the rs1858830 C variant in the promoter region of theMETgene is associated with autistic disorder
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