54 related articles for article (PubMed ID: 38463082)
1. Autosomal Recessive Spastic Paraplegia and Psychomotor Retardation With or Without Seizures: A Case Report From Saudi Arabia.
Alzaidan H; Alluhaybi B; Albulayhid NA; Al-Jabr KH; Alotaibi FT; Alqahtani A
Cureus; 2024 May; 16(5):e60642. PubMed ID: 38899231
[TBL] [Abstract][Full Text] [Related]
2. Molybdenum Cofactor Deficiency (MoCD) Masquerading as Stroke Like Episodes: Authors' Reply.
Gowda VK; Markose AP; Reddy VS; Srinivasan VM
Indian J Pediatr; 2024 Jul; 91(7):757. PubMed ID: 38244183
[No Abstract] [Full Text] [Related]
3. Molybdenum Cofactor Deficiency (MoCD) Masquerading as Stroke-Like Episodes: Correspondence.
Finsterer J
Indian J Pediatr; 2024 Jul; 91(7):756. PubMed ID: 38240982
[No Abstract] [Full Text] [Related]
4. A case report of molybdenum cofactor deficiency type A: the first case diagnosed in Syria.
Kardah H; Al-Zoubi H; Odeh Z; Joumaa R; Alasmar D
Ann Med Surg (Lond); 2024 Mar; 86(3):1762-1765. PubMed ID: 38463082
[TBL] [Abstract][Full Text] [Related]
5. New Neuroimaging Findings in Patients with Molybdenum Cofactor Deficiency Type A: A Case Report and Literature Review.
Liu H; Yu X; He S; Li S
Curr Med Imaging; 2024; 20():1-7. PubMed ID: 38389347
[TBL] [Abstract][Full Text] [Related]
6. [Molybdenum cofactor deficiency type B manifested as Leigh-like syndrome: a case report and literature review].
Tian XJ; Li X; Fang F; Liu ZM; Wu WJ; Liu K; Sun SZ
Zhonghua Er Ke Za Zhi; 2021 Feb; 59(2):119-124. PubMed ID: 33548958
[No Abstract] [Full Text] [Related]
7. The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A.
Yoshimura A; Kibe T; Hasegawa H; Ichida K; Koshimizu E; Miyatake S; Matsumoto N; Yokochi K
Neuropediatrics; 2019 Apr; 50(2):126-129. PubMed ID: 30695801
[TBL] [Abstract][Full Text] [Related]
8. The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with
Abe Y; Aihara Y; Endo W; Hasegawa H; Ichida K; Uematsu M; Kure S
Mol Genet Metab Rep; 2021 Mar; 26():100716. PubMed ID: 33552910
[TBL] [Abstract][Full Text] [Related]
9. Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.
Zaki MS; Selim L; El-Bassyouni HT; Issa MY; Mahmoud I; Ismail S; Girgis M; Sadek AA; Gleeson JG; Abdel Hamid MS
Eur J Paediatr Neurol; 2016 Sep; 20(5):714-22. PubMed ID: 27289259
[TBL] [Abstract][Full Text] [Related]
10. An unusual case of a toddler with Canavan disease with frequent intractable seizures: A case report and review of the literature.
Irilouzadian R; Goudarzi A; Hesami H; Sarmadian R; Biglari HN; Gilani A
SAGE Open Med Case Rep; 2023; 11():2050313X231160885. PubMed ID: 36968992
[TBL] [Abstract][Full Text] [Related]
11. Molybdenum Cofactor Deficiency in Humans.
Johannes L; Fu CY; Schwarz G
Molecules; 2022 Oct; 27(20):. PubMed ID: 36296488
[TBL] [Abstract][Full Text] [Related]
12. A neonate with molybdenum cofactor deficiency type B.
Lin Y; Liu Y; Chen S; Zhu J; Huang Y; Lin Z; Chen S
Transl Pediatr; 2021 Apr; 10(4):1039-1044. PubMed ID: 34012852
[TBL] [Abstract][Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
