Results
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461.
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462.
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463.
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464.
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465.
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466.
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Biochemical, molecular and outcome analysis of eight chinese asymptomatic individuals with methyl malonic acidemia detected through newborn screening. [electronic resource] by
- Han, Lianshu
- Wu, Shengnan
- Ye, Jun
- Qiu, Wenjuan
- Zhang, Huiwen
- Gao, Xiaolan
- Wang, Yu
- Gong, Zhuwen
- Jin, Jing
- Gu, Xuefan
Producer: 20160614
In:
American journal of medical genetics. Part A vol. 167A
Availability: No items available.
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467.
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468.
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469.
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470.
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Cobalamin deficiency results in an abnormal increase in L-methylmalonyl-co-enzyme-A mutase expression in rat liver and COS-7 cells. [electronic resource] by
- Nakao, Motoyuki
- Hironaka, Shoko
- Harada, Naoki
- Adachi, Tetsuya
- Bito, Tomohiro
- Yabuta, Yukinori
- Watanabe, Fumio
- Miura, Takumi
- Yamaji, Ryoichi
- Inui, Hiroshi
- Nakano, Yoshihisa
Producer: 20090917
In:
The British journal of nutrition vol. 101
Availability: No items available.
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471.
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472.
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473.
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474.
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475.
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476.
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Tonsils of the soft palate do not mediate the response of pigs to oral vaccination with heat-inactivated Mycobacterium bovis. [electronic resource] by
- Beltrán-Beck, Beatriz
- Romero, Beatriz
- Boadella, Mariana
- Casal, Carmen
- Bezos, Javier
- Mazariegos, María
- Martín, MariPaz
- Galindo, Ruth C
- Pérez de la Lastra, José M
- Villar, Margarita
- Garrido, Joseba M
- Sevilla, Iker A
- Asensio, Fernando
- Sicilia, Javier
- Lyashchenko, Konstantin P
- Domínguez, Lucas
- Juste, Ramón A
- de la Fuente, José
- Gortázar, Christian
Producer: 20150416
In:
Clinical and vaccine immunology : CVI vol. 21
Availability: No items available.
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477.
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478.
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The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis. [electronic resource] by
- Suormala, Terttu
- Baumgartner, Matthias R
- Coelho, David
- Zavadakova, Petra
- Kozich, Viktor
- Koch, Hans Georg
- Berghaüser, Martin
- Wraith, James E
- Burlina, Alberto
- Sewell, Adrian
- Herwig, Jürgen
- Fowler, Brian
Producer: 20041124
In:
The Journal of biological chemistry vol. 279
Availability: No items available.
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479.
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Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group. [electronic resource] by
- Merinero, B
- Pérez, B
- Pérez-Cerdá, C
- Rincón, A
- Desviat, L R
- Martínez, M A
- Sala, P Ruiz
- García, M J
- Aldamiz-Echevarría, L
- Campos, J
- Cornejo, V
- Del Toro, M
- Mahfoud, A
- Martínez-Pardo, M
- Parini, R
- Pedrón, C
- Peña-Quintana, L
- Pérez, M
- Pourfarzam, M
- Ugarte, M
Producer: 20080623
In:
Journal of inherited metabolic disease vol. 31
Availability: No items available.
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480.
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