statistiche ricercatore

Nome	#
Fragile X syndrome : A review of clinical and molecular diagnoses, file dfa8b999-fde6-748b-e053-3a05fe0a3a96	159
MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions, file dfa8b998-3bfe-748b-e053-3a05fe0a3a96	140
A Clinical-Based Diagnostic Approach to Cerebellar Atrophy in Children, file dfa8b9a6-0e95-748b-e053-3a05fe0a3a96	49
Pediatric Slow-Progressive, but Not Non-Progressive Cerebellar Ataxia Delays Intra-Limb Anticipatory Postural Adjustments in the Upper Arm, file 2ec8fb5f-c8ec-467c-9989-d142bb77bb7c	33
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b998-7e25-748b-e053-3a05fe0a3a96	4
16p13 microduplication without CREBBP involvement : moving toward a phenotype delineation, file dfa8b997-f928-748b-e053-3a05fe0a3a96	3
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review, file dfa8b99d-c5ce-748b-e053-3a05fe0a3a96	2
Comparison of three therapeutic regimens for genotype-3 hepatitis C virus infection in a large real-life multicentre cohort, file dfa8b9a1-e9a0-748b-e053-3a05fe0a3a96	2
Totale	392

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	7	0	0	0	0	0	0	0	0	0	0	7	0
2019/2020	79	2	0	4	16	8	9	6	9	12	4	4	5
2020/2021	51	3	3	1	4	4	3	10	3	4	3	9	4
2021/2022	68	2	6	2	4	8	0	7	4	3	5	19	8
2022/2023	109	0	0	17	12	1	8	0	20	38	6	7	0
2023/2024	48	0	3	7	1	2	5	13	4	5	3	5	0
Totale													392

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