Results 131 to 140 of about 19,992,265 (173)

Diagnosis of cobalamin C deficiency with renal abnormality from onset in a Chinese child by next generation sequencing: A case report. [PDF]

Exp Ther Med, 2017
Chen Q, Bao H, Wu H, Zhao S, Huang S, Zhao F.   +5 more
europepmc   +1 more source

Identification of <i>CD320</i>-Associated Cobalamin Transport Deficiency Through Newborn Screening Caused by Novel Homozygous Candidate Variants. [PDF]

Genes (Basel)
Almalki F, Alsofyany AS, Almalki AK, Abu Shuaylan AO, Alruqi H, Althobiti JM.   +5 more
europepmc   +1 more source

The Dynamic Coenzyme Network of B Vitamins in Nutritional Neuropathy and Neuropsychiatric Vulnerability: A Mechanistic Narrative Review. [PDF]

Nutrients
Yoon Y, Hwang J, Park R, Shim J, Lam KHS, de Castro JC, Suryadi T, Suhaimi A, Yang CM.   +8 more
europepmc   +1 more source

Revisiting the hematological manifestations of vitamin B12 deficiency. [PDF]

Front Nutr
Parakh N, Dewan P.
europepmc   +1 more source

Characteristic MRI findings of nitrous oxide-induced subacute combined degeneration despite low-normal vitamin B12 levels. [PDF]

Radiol Case Rep
Mustaquim B, Ahmed A, Haque MZ, Siddiqui M.   +3 more
europepmc   +1 more source

Homocystinuria symptomatology collected through an international patient-report data program as a source for natural history data. [PDF]

Mol Genet Metab Rep
Parke B, Bartke D, Beek G, Talebizadeh Z, Chapman KA, Baker J, Thomas JA.   +6 more
europepmc   +1 more source

Comparative efficacy of vitamin B12 supplementation routes in adults with replacement indication: a systematic review. [PDF]

EClinicalMedicine
Debone D, Azeredo da Silva AF, Cordenonssi JT, Cohen RV.   +3 more
europepmc   +1 more source

Pernicious Anemia: Basic Pathophysiology and Diagnostic Challenges in Neuropsychiatric Patients. [PDF]

Hematol Rep
Myat YM, Thein KZ, Oo TH.
europepmc   +1 more source

Exploration of Metabolic Alterations in Methylmalonic Acidemia across Distinct Genetic Backgrounds. [PDF]

ACS Omega
Zhi HJ, Ding Y, Deng YX, Chen T, Cao Y, Chang SY, Zhan X, Xu F, Hao LL, Liang LL, Qiu WJ, Zhang HW, Gu XF, Han LS.   +13 more
europepmc   +1 more source

Case Report: Persistent isolated hyperhomocysteinemia in an adolescent with celiac disease and homozygous <i>MTHFR</i> c.665C>T polymorphism: a multifactorial disturbance of one-carbon metabolism. [PDF]

Front Genet
Al Masseri Z, Marshall CR, Martin N, Cordeiro D, Guilder L, Inbar-Feigenberg M.   +5 more
europepmc   +1 more source