![Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley](https://onlinelibrary.wiley.com/cms/asset/e5de7842-12d0-4771-abac-e5bbc7ee40d7/jimd12338-fig-0003-m.jpg)
Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley
Homocystinuria - HCU Network Australia - On Tuesday 30 November, HCU Network Australia together with E-HOD will host the 4th International Homocystinurias Patient Expert Meeting. Registration for the virtual event is free.
![PDF) Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis PDF) Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis](https://i1.rgstatic.net/publication/364462463_Human_ultrarare_genetic_disorders_of_sulfur_metabolism_demonstrate_redundancies_in_H2S_homeostasis/links/6359764212cbac6a3efb1ff1/largepreview.png)
PDF) Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis
![Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley](https://onlinelibrary.wiley.com/cms/asset/1126f600-7e7b-444e-b073-45edeb645929/jimd12338-fig-0001-m.jpg)
Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis - Kožich - 2021 - Journal of Inherited Metabolic Disease - Wiley
![Jan BULTAS | Prof., MD, PhD. | Charles University in Prague, Prague | CUNI | Department of Pharmacology (3. LF) | Research profile Jan BULTAS | Prof., MD, PhD. | Charles University in Prague, Prague | CUNI | Department of Pharmacology (3. LF) | Research profile](https://i1.rgstatic.net/ii/profile.image/276895737368578-1443028496739_Q512/Jan-Bultas.jpg)
Jan BULTAS | Prof., MD, PhD. | Charles University in Prague, Prague | CUNI | Department of Pharmacology (3. LF) | Research profile
![Viktor KOZICH | Professor (Full) | Professor, MD, PhD | Charles University in Prague, Prague | CUNI | Department of Pediatrics and Adolescent Medicine (1. LF) | Research profile Viktor KOZICH | Professor (Full) | Professor, MD, PhD | Charles University in Prague, Prague | CUNI | Department of Pediatrics and Adolescent Medicine (1. LF) | Research profile](https://www.researchgate.net/profile/Viktor-Kozich/publication/349650659/figure/tbl1/AS:996540038512642@1614605068483/Characteristics-information-products-in-different-European-countries-1_Q320.jpg)
Viktor KOZICH | Professor (Full) | Professor, MD, PhD | Charles University in Prague, Prague | CUNI | Department of Pediatrics and Adolescent Medicine (1. LF) | Research profile
![Viktor KOZICH | Professor (Full) | Professor, MD, PhD | Charles University in Prague, Prague | CUNI | Department of Pediatrics and Adolescent Medicine (1. LF) | Research profile Viktor KOZICH | Professor (Full) | Professor, MD, PhD | Charles University in Prague, Prague | CUNI | Department of Pediatrics and Adolescent Medicine (1. LF) | Research profile](https://www.researchgate.net/profile/Urh-Groselj/publication/349836055/figure/fig1/AS:998299779747840@1615024623022/Map-of-the-International-Society-for-Neonatal-ISNS-European-region-colour-coded-by-the_Q320.jpg)