Skip to main content

5 articles related to "Hhh"

No matches to your query could be found. Try another search term.
No matches to your query could be found. Try another search term.
No matches to your query could be found. Try another search term.
No matches to your query could be found. Try another search term.
No matches to your query could be found. Try another search term.

Articles

Original Research

Published on 24 Nov 2022

Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene

in Genetics of Common and Rare Diseases

Imad Dweikat
Reham Khalaf-Nazzal

Frontiers in Genetics

doi 10.3389/fgene.2022.1004598

4,390 views
5 citations

Case Report

Published on 27 May 2022

Immune Alterations in a Patient With Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome: A Case Report

in Primary Immunodeficiencies

Silene M. Silvera-Ruiz
Corinne Gemperle
Natalia Peano
Valentina Olivero
Adriana Becerra
Johannes Häberle
Adriana Gruppi
Laura E. Larovere
Ruben D. Motrich

Frontiers in Immunology

doi 10.3389/fimmu.2022.861516

5,433 views
5 citations

Original Research

Published on 11 Jul 2022

Germplasm Sources, Genetic Richness, and Population Differentiation of Modern Chinese Soybean Cultivars Based on Pedigree Integrated With Genomic-Marker Analysis

in Plant Bioinformatics

Chunyan Li
Wubin Wang
Yongpeng Pan
Fangdong Liu
Jianbo He
Chuanxiang Liu
Jiqiu Cao
Xiaoyan Zhang
Jinming Zhao
Junyi Gai

Frontiers in Plant Science

doi 10.3389/fpls.2022.945839

3,554 views
4 citations

Original Research

Published on 03 Aug 2021

Performances of Whole Tumor Texture Analysis Based on MRI: Predicting Preoperative T Stage of Rectal Carcinomas

in Cancer Imaging and Image-directed Interventions

Jia You
Jiandong Yin

Frontiers in Oncology

doi 10.3389/fonc.2021.678441

3,424 views
22 citations

Mini Review

Published on 22 Feb 2019

Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle Metabolism

in Movement Disorders

Emanuele Panza
Diego Martinelli
Pamela Magini
Carlo Dionisi Vici
Marco Seri

Frontiers in Neurology

doi 10.3389/fneur.2019.00131

11,297 views
32 citations