Zobrazeno 1 - 10
of 230
pro vyhledávání: '"R. Bieth"'
Autor:
Bakhat, Khush1 khushbkht@gmail.com, Mateen, Irsa2 irsamateen.biochem@mul.edu.pk, Saif, Hina3 hina.saif@deaht.uol.edu.pk, Anwar, Kanwal1 kanwalanwar14@gmail.com, Sarfraz, Sadaf1 sadafsarfraz.40@gmail.com, Javaid, Sheza1 shezajavaid930@gmail.com, Khaleeq-ur-Rehman4 khaleeqr@hotmail.com, Arshad, Adnan1 adnanarshad@fccollege.edu.pk, Mustafa, Muhammad1 muhammadmustafa@fccollege.edu.pk
Publikováno v:
Archives of Italian Urology & Andrology / Archivio Italiano di Urologia Andrologia. Sep2024, Vol. 96 Issue 3, p1-7. 7p.
Autor:
Mingarelli, Alessia1 (AUTHOR), Pipitone, Giovanni Battista2 (AUTHOR), Torini, Giacomo3 (AUTHOR), Patricelli, Maria Grazia2 (AUTHOR), Totaro, Martina1 (AUTHOR), Colonna, Clara1 (AUTHOR), Carrera, Paola2,3 (AUTHOR), Raviglione, Federico1 (AUTHOR)
Publikováno v:
Case Reports in Genetics. 9/30/2023, p1-5. 5p.
Publikováno v:
Annales de biologie clinique. 40(5)
A new, clinically and biochemically atypical case of Lesch-Nyhan syndrome is presented. There is mild neurological involvement, the APRTase activity is normal, despite a raised PRPP concentration and HGPRTase activity is low. The optimal pH and tempe
Publikováno v:
La Nouvelle presse medicale. 8(49)
Publikováno v:
Pediatrie. 32(5)
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 75(12)
Histological changes of the skeletal muscle with moderate fatty infiltration and varied abnormalities of the muscle fibres and conjunctivo-vascular tissue were demonstrated in three adult patients with apparently primary cardiomyopathy with dilatatio
Publikováno v:
Archives francaises de pediatrie. 35(5)
Studies of a child with hyperammonemia have demonstrated a deficiency in OCTase. The kinetic properties of the enzyme were studied and it could be shown that we have to deal with a new mutation which is different from the ones previously known. It is
Publikováno v:
La Nouvelle presse medicale. 5(40)
Publikováno v:
Annales de pediatrie. 27(10)
Publikováno v:
Annales de pediatrie. 27(4)