about
Motor Learning as Young Gymnast's Talent Indicator.HLA related genetic risk for coeliac disease.Increased prevalence of celiac disease without gastrointestinal symptoms in adults MICA 5.1 homozygous subjects from the Campania area.Efficacy of aerobic physical retraining in a case of combined pulmonary fibrosis and emphysema syndrome: a case report.Psychological well-being and social participation assessment in visually impaired subjects playing Torball: a controlled study.Molecular analysis of the adiponectin gene in severely obese patients from southern Italy.Detachable snare versus epinephrine injection in the prevention of postpolypectomy bleeding: a randomized and controlled study.Pseudouridine and 1-ribosylpyridin-4-one-3-carboxamide (PCNR) serum concentrations in human immunodeficiency virus type 1-infected patients are independent predictors for AIDS progression.Prenatal diagnosis of inherited diseases: 20 years' experience of an Italian Regional Reference Centre.Mental health and social participation skills of wheelchair basketball players: a controlled study.Use of video observation and motor imagery on jumping performance in national rhythmic gymnastics athletes.Effects of resistance training on jumping performance in pre-adolescent rhythmic gymnasts: a randomized controlled study.Improving neuromuscular performance in young basketball players: plyometric vs. technique training.Sprint vs. intermittent training in young female basketball players.Effects of different types of physical activity on the cognitive functions and attention in older people: A randomized controlled study.ACE and AGTR1 Polymorphisms in Elite Rhythmic GymnasticsFOXN1 mutation abrogates prenatal T-cell development in humansAscitic pseudouridine discriminates between hepatocarcinoma-derived ascites and cirrhotic ascitesQuantitative analysis of aldolase A mRNA in liver discriminates between hepatocellular carcinoma and cirrhosisMultiplex PCR typing of the three most frequent HLA alleles in celiac diseaseEfficiency of two different nine-loci short tandem repeat systems for DNA typing purposesFOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetusHolt-Oram syndrome associated with anomalies of the feetAcute effects of whole-body vibration on running gait in marathon runnersUphill racewalking at iso-efficiency speed
P50
Q34528787-2F1E7024-20D6-43C8-B521-19912877C825Q35956063-4C762611-1918-4CCB-AA46-A20751A781D2Q38293438-82F1BE58-E5C6-474B-B67C-2D2B05764101Q40363377-6E441D4B-FCB1-4B10-98BB-626CA6594F4AQ44506991-9E29B79A-519D-44E4-982D-F3CC29CCE7D5Q44856930-F482EB2D-AB94-4810-9DAF-F50611C248CEQ45081851-0EEF2528-AF9D-44AE-9558-0DA4F9504C27Q45116173-887C7936-8D88-4FEA-8985-E011C1533A7FQ46022948-B69D9B08-4148-4600-A13B-84A7808EF7A4Q47981900-F2BB5CF1-19F6-4DB8-AFDA-1C7AF5D6EED2Q50608981-262119CB-FB87-4911-89EC-6F0AA2A14B77Q51105030-955B4A12-B106-4C2B-8E02-1E1518AC3A60Q51134771-FE11AC6C-0849-4B41-B57A-3AE13F254CA2Q51162175-39439965-3026-4BAB-95C2-299214C88C65Q53422378-B7B0C8AA-1EA1-4228-8BC6-0DE0250C7102Q59277554-9D913E04-C558-4EBA-9C2A-6938E0D6F478Q61696152-602DFBE6-5416-4937-BC1F-80E5AE0F5289Q71754326-1BAE4B28-BBD7-4FF8-A8B3-AEBE644C599CQ74000435-5469C6C8-E4FC-4CF7-9C13-EEA0F281D0FFQ74347937-8932F7EE-511A-453D-9CA6-B5859AEAD484Q77945369-24E1F64F-98ED-4BD7-8648-2B856B9F9552Q80867212-9E04C573-ECBB-4594-8C85-59456159F504Q80900694-84D57133-FDFC-4BCA-8056-29E05722A68AQ87371517-E0E96E2F-4C47-4480-BF30-6E444ED518C1Q87411600-69BC0DF7-C5B3-4CDD-A4A2-A97E37E8F37D
P50
description
researcher ORCID ID = 0000-0003-4680-1535
@en
wetenschapper
@nl
name
Giuseppe Calcagno
@ast
Giuseppe Calcagno
@en
Giuseppe Calcagno
@es
Giuseppe Calcagno
@nl
type
label
Giuseppe Calcagno
@ast
Giuseppe Calcagno
@en
Giuseppe Calcagno
@es
Giuseppe Calcagno
@nl
prefLabel
Giuseppe Calcagno
@ast
Giuseppe Calcagno
@en
Giuseppe Calcagno
@es
Giuseppe Calcagno
@nl
P106
P1153
7004221028
P21
P31
P496
0000-0003-4680-1535