Suchergebnisse - "Reza Azizi"

PubPharm (43)

1

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

enthalten in: American journal of human genetics | 2019

von Dias, C. | Punetha, J. | Zheng, C. | +40

2

Prognostic factors in patients with active non-variceal upper gastrointestinal bleeding

enthalten in: Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology | 2019

von Hajiagha Mohammadi, A. | Reza Azizi, M.

3

Body mass index growth trajectories from birth through 24 months in Iranian infants of mothers with gestational diabetes mellitus

enthalten in: Diabetes & metabolic syndrome | 2019

von Nouhjah, S. | Shahbazian, H. | Latifi, S. | +2

4

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking

in: Frontiers in Neuroscience | 2019

von Haicui Wang | Haicui Wang | Ayşe Kaçar Bayram | +33

5

Hemi-ESES associated with agenesis of the corpus callosum and normal cognition

enthalten in: Epilepsy & behavior case reports | 2019

von Mohammadi, M. | Kowkabi, S. | Asadi-Pooya, A. | +2

6

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2018

von Helal, M. | Mazaheri, N. | Shalbafan, B. | +13

7

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

enthalten in: Neurological sciences | 2018

von Helal, M. | Mazaheri, N. | Shalbafan, B. | +13

8

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

enthalten in: Neurological sciences | 2018

von Helal, M. | Mazaheri, N. | Shalbafan, B. | +13

9

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

enthalten in: Neurological sciences | 2018

von Helal, M. | Mazaheri, N. | Shalbafan, B. | +13

10

Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration

enthalten in: Neurology | 2018

von Muto, V. | Flex, E. | Kupchinsky, Z. | +28

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