8. Sayfa - Nobel Tıp Kitabevleri

Tüm Sayfalar

1. Ajanovic S, Jobst B, Jiménez J, Quesada R, et al. Non-invasive meningitis screening in neonates and infants: multicentre international study. Clinical Research Article. 2025;1–11. 2. Al-Qahtani SM, Shati AA, Alqahtani YA, Ali AS. Etiology, clinical phenotype ...

1. Adelson PD, Wisniewski SR, Beca J, Brown SD, Bell M, Mui zelaar JP et al (2013) Comparison of hypothermia and normo thermia after severe traumatic brain injury in children (Cool Kids): a phase 3, randomised controlled trial. Lancet Neurol 12(6):546–553. 2. Ayl ...

1. Bachmann-Gagescu R, Dempsey JC, Phelps IG, et al. Healthcare recommendations for Joubert syndrome. Am J Med Genet A. 2020;182(10):2293-2308. doi:10.1002/ajmg.a.61399 2. Bender F, Synofzik M, Schöls L, et al. Natural history of polymerase gamma–related ataxia. Mo ...

1. Ashwal S, Gropman AL, Finkel RS, Schor NF, Ferriero DM, Gropman AL, et al. The cerebellum and the hereditary ataxias. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, Finkel RS, Gropman AL, editors. Swaiman’s Pediatric Neurology: Principles and Practice. 6th ed. Phil ...

1. Arnold M. Headache classification committee of the international headache society (IHS) the international classification of headache disorders. Cephalalgia. 2018;38(1):1-211. 2. Beretti T, Desnous B. Vertigo and dizziness in children: When to consider a neurolog ...

1. Baumann P, Myllylä VV, Leisti J. Myotonia congenita in northern Finland: an epidemiological and genetic study. J Med Genet. 1998;35(4):293–296. doi:10.1136/jmg.35.4.293. 2. Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, et al. Molecul ...

1. Abicht A, Muller JS, Lochmuller H. Congenital Myasthenic Syndromes Overview. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews((R)). Seattle (WA)1993. 2. Arredondo J, Lara M, Gospe Jr. SM, Mazia CG, Vaccarezza M, Garcia-Er ...

1. Calucho M, Bernal S, Alías L, March F, Venceslá A, Rodríguez-Álvarez FJ, vd. Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases. Neuromuscular Disorders. 01 Mart 2018;2 ...

1. Bartels B, Montes J, van der Pol WL, de Groot JF. Physical exercise training for type 3 spinal muscular atrophy. Cochrane Database Syst Rev. 2019;(3):CD012120. doi:10.1002/14651858.CD012120.pub2 2. Birnkrant DJ, Bushby K, Bann CM, et al. Diagnosis and manageme ...

1. Abdel-Mannan O, D'Argenzio L, Pitt M, et al. Two cases of Guillain-Barré syndrome variants presenting with dysautonomia. Child Neurol Open. 2019;6:2329048X19856778. 2. Agrawal S, Peake D, Whitehouse WP. Management of children with Guillain-Barré syndrome. Arch ...

1. Absoud M, Greenberg BM, Lim M, Lotze T, Thomas T, Deiva K. Pediatric transverse myelitis. Neurology. 2016;87(9 Suppl 2):S46-S52. doi:10.1212/WNL.0000000000002820 2. Akaishi T, Sato DK, Nakashima I, et al. MRI and retinal abnormalities in isolated optic neuriti ...

1. Abdel Razek AA, Abd El-Gaber N, Abdalla A, et al. Apparent diffusion coefficient vale of the brain in patients with Gaucher's disease type II and type III. Neuroradiology. 2009;51(11):773-779. doi:10.1007/s00234-009-0548-1 2. Adachi M, Schneck L, Cara J, et al ...

1. Ahn JH, Kim AR, Lee C, et al. Type 1 Sialidosis Patient With a Novel Deletion Mutation in the NEU1 Gene: Case Report and Literature Review. Cerebellum. 2019;18(3):659-664. doi:10.1007/S12311-019-1005-2 2. Al-Saady M, Beerepoot S, Plug BC, et al. Neurodegenerat ...

1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th ed, text revision (DSM-5-TR). Washington, DC: American Psychiatric Association; 2022. 2. Butler MG, Dasouki MJ, Zhou XP, et al. Subset of individuals with autism spec ...

1. Alamri MM, Alrehaili MA, Albariqi W. Relationship Between Speech Delay and Smart Media in Children: A Systematic Review. Cureus. 2023 Sep 17;15(9):e45396. doi: 10.7759/cureus.45396. PMID: 37854747; PMCID: PMC10580299. 2. American Academy of Pediatrics. ( ...

1. Abukhaled M, Al Muqbil M, Alghamdi MA, Hundallah K, Suleiman J, Ben-Omran T, et al. Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review. Eur J Pediatr. 2023;182(6):2535–45. 2. Blau N, Hennermann J ...

1. Albanese A, Bhatia K, Bressman SB, et al. Phenomenology and classification of dystonia: A consensus update. Mov Disord. 2013;28(7):863-873. doi:10.1002/mds.25475 2. Albanese A, Valente EM, Romito LM, Bellacchio E, Elia AE, Dallapiccola B. The PINK1 phenotype c ...

1. Bernard TJ, Rivkin MJ. Arterial ischemic stroke. In: Swaiman KF, Ashwal S, Ferriero DM, et al, eds. Swaiman’s Pediatric Neurology: Principles and Practice. 9th ed. Elsevier; 2025: Part XVII. 2. Beslow LA, Licht DJ, Smith SE, et al. Predictors of outcome in chi ...

1. Adde L, Wu Y, Gao H, Zhang D, Yin C. Early prediction of cerebral palsy using video-based artificial intelligence analysis of spontaneous movements in infants. Nat Commun. 2021;12(1):7232. doi:10.1038/s41467-021-27555-3 2. Benninger DH, Berman BD, Hallett ...

1. Abbassi-Ghanavati M, Alexander JM, McIntire DD et al. Neonatal effects of magnesium sulfate given to the mother. Obstet Gynecol. 2012;119(1):59–65. doi:10.1097/AOG.0b013e31823b3c3a 2. Abicht A, Müller JS, Lochmüller H et al. Congenital myasthenic syndromes. In: ...

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