Suchergebnisse - "Giannotti, A"

PubPharm (182)

1

Neural stimulation hardware for the selective intrafascicular modulation of the vagus nerve

enthalten in: bioRxiv.org | 2024

von Strauss, I. | Agnesi, F. | Zinno, C. | +14

2

Decoding bladder state from pudendal intraneural signals in pigs

enthalten in: APL bioengineering | 2023

von Giannotti, A. | Lo Vecchio, S. | Musco, S. | +15

3

Neural Stimulation Hardware for the Selective Intrafascicular Modulation of the Vagus Nerve

enthalten in: IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society | 2023

von Strauss, I. | Agnesi, F. | Zinno, C. | +14

4

Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome)

enthalten in: Clinical genetics | 2003

von Digilio, M. | Giannotti, A. | Dallapiccola, B. | +1

5

Deletion of the SHOX gene in patients with short stature of unknown cause

enthalten in: American journal of medical genetics. Part A | 2003

von Morizio, E. | Stuppia, L. | Gatta, V. | +10

6

Impact of antiviral treatment on recurrence of hepatitis B virus infection and disease

enthalten in: Transplantation proceedings | 2003

von Ciccorossi, P. | Filipponi, F. | Oliveri, F. | +7

7

Recurrence of HCV infection in liver transplant patients : evaluation of IgM anti-HCV and IgM anti-CMV

enthalten in: Transplantation proceedings | 2003

von Ceccherini-Nelli, L. | Giannotti, A. | Malizia, T. | +9

8

Spectrum of clinical variability in familial deletion 22q11.2 : from full manifestation to extremely mild clinical anomalies

enthalten in: Clinical genetics | 2003

von Digilio, M. | Angioni, A. | De Santis, M. | +4

9

SHOX mutations detected by FISH and direct sequencing in patients with short stature

enthalten in: Journal of medical genetics | 2003

von Stuppia, L. | Calabrese, G. | Gatta, V. | +14

10

Short Report. Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies

enthalten in: Clinical genetics | 2003

von Digilio, M. | Angioni, A. | De Santis, M. | +4

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