Yoshiaki Saito

K. Sugiyama, Yoshiaki Saito, A. Kobayashi, 2012, Ophthalmic surgery, lasers & imaging : the official journal of the International Society for Imaging in the Eye.

Unusual exocrine complication of pancreatitis in mitochondrial disease

I. Nishino, Yu‐ichi Goto, M. Sasaki, 2013, Brain and Development.

Inflammatory changes in infantile-onset LMNA-associated myopathy

I. Nonaka, Y. Hayashi, I. Nishino, 2011, Neuromuscular Disorders.

Three cases of right frontal megalencephaly: Clinical characteristics and long-term outcome

S. Fujii, Y. Maegaki, J. Tohyama, 2016, Brain & development (Tokyo. 1979).

Heme oxygenase-1, a potential biomarker of chronic silicosis, attenuates silica-induced lung injury.

Y. Nagashima, Takashi Sato, Y. Ishigatsubo, 2006, American journal of respiratory and critical care medicine.

Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama‐type congenital muscular dystrophy brain

M. Mizuguchi, S. Takashima, Yoshiaki Saito, 2000, Annals of neurology.

Muscle glycogen storage disease 0 presenting recurrent syncope with weakness and myalgia

Y. Hayashi, I. Nishino, W. Liang, 2012, Neuromuscular Disorders.

Familial limb pain in childhood: Unusual manifestation of migraine?

T. Takeshima, K. Ohno, Yoshiaki Saito, 2006, Brain and Development.

Progression from near-normal to end-stage lungs in chronic interstitial pneumonia related to silica exposure: long-term CT observations.

Y. Kaji, N. Suganuma, K. Fujimoto, 2008, AJR. American journal of roentgenology.

Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data

S. Kanai, T. Okanishi, Y. Maegaki, 2021, Frontiers in Neurology.

Chronobiometric Assessment of Autogenic Training Effects upon Blood Pressure and Heart Rate

G. Cornelissen, F. Halberg, K. Otsuka, 1996, Perceptual and motor skills.

Improvement in Behavioral Problems in Children with Intractable Epilepsy Using the Child Behavior Checklist after Surgical Intervention

A. Takahashi, Y. Inoue, M. Kaga, 2011 .

Postnatal evolution of cortical malformation in the “non-affected” hemisphere of hemimegalencephaly

M. Sasaki, T. Otsuki, E. Nakagawa, 2010, Brain and Development.

Arthrogryposis multiplex congenita with callosal agenesis and dentato-olivary dysplasia

Yayoi Miyazono, K. Ohno, Yoshiaki Saito, 2006, Brain & development (Tokyo. 1979).

Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata.

Y. Maegaki, H. Nagashima, T. Okazaki, 2016, Pediatric neurology.

Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome

T. Matsuishi, S. Takashima, K. Hamano, 2001, Brain and Development.

Pontine malformation, undecussated pyramidal tracts, and regional polymicrogyria: a new syndrome.

E. Engle, Y. Nakata, Toshiyuki Yamamoto, 2014, Pediatric neurology.

Serum Heme Oxygenase-1 as a Marker of Lung Function Decline in Patients With Chronic Silicosis

Takashi Sato, T. Shimosato, Y. Ishigatsubo, 2012, Journal of occupational and environmental medicine.

Vessel wall enhancement in the diagnosis and management of primary angiitis of the central nervous system in children

S. Fujii, Y. Maegaki, E. Yamashita, 2016, Brain and Development.

Short-lasting unilateral neuralgiform headache attacks with ispilateral facial flushing is a new variant of paroxysmal extreme pain disorder

S. Manaka, N. Matsumoto, M. Shiina, 2015, The Journal of Headache and Pain.

Hyperzincemia with systemic inflammation: a heritable disorder of calprotectin metabolism with rheumatic manifestations?

Kayoko Saito, M. Moriya, S. Manno, 2002, The Journal of pediatrics.

Dravet syndrome with parkinsonian symptoms and intact dopaminergic neurons: A case report

R. Hanajima, Y. Maegaki, Yoshiaki Saito, 2020, Brain and Development.

Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination

Y. Matsubara, Y. Aoki, M. Sasaki, 2011, Brain and Development.

Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome

M. Kubota, M. Sasaki, K. Kurosawa, 2011, Brain and Development.

A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement

I. Nonaka, Y. Hayashi, I. Nishino, 2012, Neuromuscular Disorders.

Effect of total callosotomy on KCNQ2-related intractable epilepsy

N. Matsumoto, S. Miyatake, S. Takeshita, 2020, Brain and Development.

Hemiconvulsion–hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy

H. Kurahashi, M. Sasaki, E. Nakagawa, 2009, Epilepsia.

Identification of sleep hypoventilation in young individuals with Becker muscular dystrophy: A pilot study

Y. Sunada, M. Matsuo, Yuko Nakamura, 2018, Brain and Development.

Cytokine/chemokine elevation during the transition phase from HSV encephalitis to autoimmune anti-NMDA receptor encephalitis

Y. Maegaki, Yoshiaki Saito, H. Sakuma, 2017, Brain and Development.

Sporadic hemiplegic migraine presenting as acute encephalopathy

Yasuhiro Suzuki, T. Wada, Yoshiaki Saito, 2012, Brain and Development.

Case report Sporadic hemiplegic migraine presenting as acute encephalopathy

Yasuhiro Suzuki, T. Wada, Yoshiaki Saito, 2011 .

A pediatric patient with myopathy associated with antibodies to a signal recognition particle

Y. Hayashi, I. Nishino, M. Sasaki, 2012, Brain and Development.

Profiles of blood biomarkers in alternating hemiplegia of childhood – Increased MMP-9 and decreased substance P indicates its pathophysiology

Yu‐ichi Goto, M. Sasaki, Yoshiaki Saito, 2012, Brain and Development.

Laminar cortical necrosis in adrenal crisis: Sequential changes on MRI

Y. Maegaki, T. Ogawa, K. Ohno, 2008, Brain & development (Tokyo. 1979).

A family of distal arthrogryposis type 5 due to a novel PIEZO2 mutation

N. Matsumoto, N. Miyake, M. Sasaki, 2015, American journal of medical genetics. Part A.

Reconsideration of the diagnosis and treatment of childhood migraine: A practical review of clinical experiences

Y. Maegaki, H. Shimomura, M. Sasaki, 2017, Brain and Development.

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation

Y. Goto, M. Sasaki, E. Nakagawa, 2011, Journal of the Neurological Sciences.

Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis

E. Nanba, Y. Maegaki, M. Sasaki, 2017, Brain and Development.

Hyperzincaemia and hypercalprotectinaemia: a new disorder of zinc metabolism

B. Wolska-Kuśnierz, J. Roth, J. Beattie, 2002, The Lancet.

Ictal central apnea and bradycardia in temporal lobe epilepsy complicated by obstructive sleep apnea syndrome

Y. Maegaki, Eriko Matsuda, Yoshiaki Saito, 2015, Epilepsy & Behavior Case Reports.

Evolution of a symptomatic diffuse developmental venous anomaly with progressive cerebral atrophy in an atypical case of Sturge–Weber syndrome

H. Sugano, Shinji Itamura, Y. Maegaki, 2015, Brain and Development.

Treatment of epilepsy in severely disabled children with bilateral brain malformations

Y. Maegaki, M. Sasaki, T. Otsuki, 2009, Journal of Neurological Sciences.

Delayed neuropsychiatric syndrome in a child following carbon monoxide poisoning

Y. Maegaki, A. Seki, K. Yagi, 2007, Brain & development (Tokyo. 1979).

Intraocular pressure and visual field changes in normal-tension glaucoma patients treated using either unoprostone or latanoprost: a prospective comparative study

S. Ohkubo, T. Higashide, H. Takeda, 2017, Clinical ophthalmology.

Pharmacoresistant epileptic eyelid twitching in a child with a mutation in SYNGAP1.

S. Saitoh, E. Nanba, Y. Maegaki, 2017, Epileptic disorders : international epilepsy journal with videotape.

Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mutation.

E. Nanba, Y. Maegaki, Yuki Kawashima, 2019, Yonago acta medica.

Episodic tremors representing cortical myoclonus are characteristic in Angelman syndrome due to UBE3A mutations

K. Kikuchi, S. Saitoh, M. Sasaki, 2015, Brain and Development.

Acute encephalitis with refractory, repetitive partial seizures: Case reports of this unusual post-encephalitic epilepsy

Y. Maegaki, Yukitoshi Takahashi, K. Ohno, 2007, Brain & development (Tokyo. 1979).

Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms

M. Sasaki, E. Nakagawa, K. Sugai, 2010, Brain and Development.

Cerebellopontine calcification: a new entity of idiopathic intracranial calcification?

Yoshiaki Saito, Makoto Shibuya, Seiji Kimura, 2005, Acta Neuropathologica.

Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin: A new syndrome?

E. Nanba, Y. Maegaki, S. Moriwaki, 2008, Brain and Development.

Clinical evaluation of non-Descemet stripping automated endothelial keratoplasty (nDSAEK)

K. Sugiyama, Yoshiaki Saito, A. Kobayashi, 2012, Japanese Journal of Ophthalmology.

Beneficial effects of preoperative intravitreal bevacizumab on trabeculectomy outcomes in neovascular glaucoma

S. Ohkubo, T. Higashide, H. Takeda, 2010, Acta ophthalmologica.

High-frequency component in flash visual evoked potentials in type 3 Gaucher disease

M. Oguri, T. Okanishi, Y. Maegaki, 2019, Brain and Development.

Reassessment of phenytoin for treatment of late stage progressive myoclonus epilepsy complicated with status epilepticus

M. Sasaki, E. Nakagawa, K. Sugai, 2009, Epilepsy Research.

Brainstem neuropathology in a mouse model of Niemann–Pick disease type C

E. Ohama, H. Miyata, H. Ninomiya, 2008, Journal of the Neurological Sciences.

Neurotransmitter changes in the pathophysiology of Lesch–Nyhan syndrome

S. Takashima, Yoshiaki Saito, 2000, Brain and Development.

Basal ganglia germinoma: Diagnostic value of MR spectroscopy and 11C-methionine positron emission tomography

M. Senda, S. Fujii, H. Kamitani, 2008, Journal of the Neurological Sciences.

Ambroxol chaperone therapy for neuronopathic Gaucher disease: A pilot study

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2016, Annals of clinical and translational neurology.

Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations

I. Nonaka, Y. Hayashi, N. Laing, 2011, Neuromuscular Disorders.

Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification

S. Robertson, I. Nonaka, I. Nishino, 2009, Neuromuscular Disorders.

A mild case of giant axonal neuropathy without central nervous system manifestation

T. Shiihara, M. Sasaki, H. Takashima, 2016, Brain and Development.

Developing a mouse model of acute encephalopathy using low-dose lipopolysaccharide injection and hyperthermia treatment

M. Oguri, Y. Maegaki, Yoshiaki Saito, 2019, Experimental biology and medicine.

Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes

J. Takanashi, M. Mizuguchi, M. Kubota, 2012, Brain and Development.

Clinical and imaging characteristics of localized megalencephaly: a retrospective comparison of diffuse hemimegalencephaly and multilobar cortical dysplasia

M. Ota, Y. Tsushima, M. Sasaki, 2009, Neuroradiology.

Distinguishing Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion from Prolonged Febrile Seizures by Acute Phase EEG Spectrum Analysis

M. Oguri, Y. Maegaki, S. Hamano, 2016, Yonago acta medica.

Clinical Observation Effect of serotonin 1 A agonists and selective serotonin-reuptake inhibitors on behavioral and nighttime respiratory symptoms in Rett syndrome Running title : Serotonin therapy for Rett syndrome

Y. Maegaki, Eriko Matsuda, M. Togawa, 2016 .

Apneustic breathing in children with brainstem damage due to hypoxic–ischemic encephalopathy

M. Sasaki, T. Hashimoto, M. Fukumizu, 1999, Developmental medicine and child neurology.

Intracellular activity of superior laryngeal nerve motoneurons during fictive swallowing in decerebrate rats

K. Ezure, I. Tanaka, Yoshiaki Saito, 2002, Brain Research.

Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications

M. Kubota, K. Kosaki, Y. Maegaki, 2015, Brain and Development.

Successful treatment of migrating partial seizures in Wolf–Hirschhorn syndrome with bromide

Y. Maegaki, Toshiyuki Yamamoto, T. Okazaki, 2016, Brain and Development.

MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance.

Arthur S. Lee, D. Nickerson, M. Bamshad, 2018, American journal of human genetics.

Stimulus-induced reflex epileptic spasms in 5p− syndrome

Y. Maegaki, Yoshiaki Saito, A. Tamasaki, 2016, Brain and Development.

Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report

Y. Maegaki, S. Hirose, K. Ohno, 2018, Brain and Development.

Effects of selective serotonin re‐uptake inhibitors on behavior in Klüver–Bucy syndrome during childhood

Yoshiaki Saito, Shinichi Nishio, Atushi Yokoyama, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children

M. Sasaki, E. Nakagawa, K. Sugai, 2010, Brain and Development.

Role of the basal ganglia and thalamus in extrapontine myelinolysis and thiamine deficiency

Yoshiaki Saito, Keisuke Saeki, 2011, Brain and Development.

[Clinical characteristics of early juvenile GM2 gangliosidosis: a case report].

E. Nanba, Y. Maegaki, A. Narita, 2017, No to hattatsu = Brain and development.

Case report CD4 + CD25 high regulatory T cell in childhood ocular myasthenia gravis

M. Sasaki, E. Nakagawa, K. Sugai, 2011 .

Clinical study of asbestos-related lung cancer.

Yoshiaki Saito, T. Kishimoto, K. Ohnishi, 2003, Industrial health.

Cerebellar Ganglioglioma in Childhood: Histopathologic Implications for Management During Long-term Survival: A Case Report.

Y. Maegaki, S. Kato, Yoshiaki Saito, 2017, Yonago acta medica.

Decreased Wave V Amplitude in Auditory Brainstem Responses of Children with Cerebellar Lesions.

M. Oguri, Y. Maegaki, Yoshiaki Saito, 2018, Yonago acta medica.

Infection-associated decrease of serum creatine kinase levels in Fukuyama congenital muscular dystrophy

Takatoshi Sato, S. Takeshita, Yoshiaki Saito, 2020, Brain and Development.

Genotype–phenotype correlations in alternating hemiplegia of childhood

Akihiro Yasuhara, Hirokazu Oguni, Bo Zhang, 2014, Neurology.

8p deletion and 9p duplication in two children with electrical status epilepticus in sleep syndrome

S. Nabatame, Toshiyuki Yamamoto, M. Sasaki, 2012, Seizure.

Atypical Symptoms in Migraine-Related Alice in Wonderland Syndrome: Expansion of the Phenotype and Reflection on the Pathomechanism.

M. Oguri, Yoshiaki Saito, K. Matsuura, 2019, Yonago acta medica.

Transient encephalopathy with reversible white matter lesions: A case report

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2008, Brain & development (Tokyo. 1979).

Case report Transient encephalopathy with reversible white matter lesions: A case report

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2008 .

Laryngeal dystonia in xeroderma pigmentosum

Yoshiaki Saito, S. Kimura, H. Iwamoto, 2005, Brain and Development.

Multiple band frequency analysis in a child of medial temporal lobe ganglioglioma

Yoshiaki Saito, Taisuke Otsuki, Hirofumi Komaki, 2011, Child's Nervous System.

Electrophysiological evidence of cerebral dysfunction in childhood opsoclonus‐myoclonus syndrome

M. Kaga, M. Inagaki, M. Sasaki, 2010, Movement disorders : official journal of the Movement Disorder Society.

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy.

P. M. Nienaber, Aaron M. Beedle, J. Lueck, 2012, The Journal of clinical investigation.

Co-localization of fukutin and α-dystroglycan in the mouse central nervous system

M. Ōsawa, T. Voit, Makio Kobayashi, 2004 .

Altered glycosylation of α-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains

M. Mizuguchi, Kayoko Saito, M. Ōsawa, 2006, Brain Research.

Fukutin expression in mouse non-muscle somatic organs: its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy

M. Mizuguchi, Kayoko Saito, M. Ōsawa, 2004, Brain and Development.

Histological and ultrastructural features in the early stage of Purkinje cell degeneration in the cerebellar calcification (CC) rat.

N. Ichihara, Yoshiaki Saito, N. Wakasugi, 2004, Experimental animals.

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

M. Tominaga, H. Okuda, A. Koizumi, 2016, PloS one.

Neurodevelopmental disorders in children with macrocephaly: A prevalence study and PTEN gene analysis

E. Nanba, M. Oguri, Y. Maegaki, 2018, Brain and Development.

Effect of selenium deficiency on cardiac function of individuals with severe disabilities under long‐term tube feeding

M. Sasaki, T. Hashimoto, K. Sugai, 1998, Developmental medicine and child neurology.

Bromoderma in a patient with migrating partial seizures in infancy

S. Nabatame, M. Sasaki, E. Nakagawa, 2010, Epilepsy Research.

Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation

N. Matsumoto, H. Saitsu, M. Sasaki, 2015, Brain and Development.

Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies

M. Sasaki, K. Sugai, A. Ishiyama, 2012, Brain and Development.

A rare case of syphilis with primary complex in the lip and submaxillary region

H. Tanzawa, Yoshiaki Saito, K. Okamoto, 1990 .

Morphology of the decrementing expiratory neurons in the brainstem of the rat

K. Ezure, I. Tanaka, Yoshiaki Saito, 2002, Neuroscience Research.

K. Ezure, I. Tanaka, Yoshiaki Saito, 2002, The Journal of physiology.

[Clinical results of selective laser trabeculoplasty as adjunctive treatment for primary open-angle glaucoma patients].

T. Higashide, K. Sugiyama, Yoshiaki Saito, 2007, Nippon Ganka Gakkai zasshi.

Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2007, Brain and Development.

Long‐term prognosis of epilepsy in patients with cerebral palsy

Hisashi Noma, Yoshiaki Saito, Yoshihiro Maegaki, 2019, Developmental medicine and child neurology.

Effects of donepezil and serotonin reuptake inhibitor on acute regression during adolescence in Down syndrome

Y. Maegaki, Yukitoshi Takahashi, T. Kondoh, 2016, Brain and Development.

Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report

I. Nishino, Y. Maegaki, A. Ohtake, 2015, Brain and Development.

A case of bulbar type cerebral palsy: Representative symptoms of dorsal brainstem syndrome

Toshiyuki Yamamoto, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

Activity of neurons in ventrolateral respiratory groups during swallowing in decerebrate rats

M. Ōsawa, K. Ezure, I. Tanaka, 2003, Brain and Development.

Axonal projections of pulmonary slowly adapting receptor relay neurons in the rat

K. Ezure, I. Tanaka, Yoshiaki Saito, 2002, The Journal of comparative neurology.

Clinical factors related to recurrence of anterior segment neovascularization after treatment including intravitreal bevacizumab.

S. Ohkubo, T. Higashide, H. Takeda, 2010, American journal of ophthalmology.

Subfoveal choroidal thickness change following segmental scleral buckling for rhegmatogenous retinal detachment.

T. Higashide, K. Sugiyama, Yoshiaki Saito, 2012, American journal of ophthalmology.

Efficacy of primary silicone oil tamponade for the treatment of retinal detachment caused by macular hole in high myopia.

K. Sugiyama, Yoshiaki Saito, M. Kimura, 2011, American journal of ophthalmology.

Reflections on the brainstem dysfunction in neurologically disabled children

Yoshiaki Saito, 2009, Brain and Development.

Adverse events associated with intraocular injections of bevacizumab in eyes with neovascular glaucoma

S. Ohkubo, T. Higashide, K. Sugiyama, 2012, Graefe's Archive for Clinical and Experimental Ophthalmology.

Conjunctival vasculature patterns influencing the filtering bleb shape following trabeculectomy with limbal-based conjunctival flaps

M. Aihara, T. Higashide, K. Sugiyama, 2009, Japanese Journal of Ophthalmology.

Acute encephalitis with refractory, repetitive partial seizures (AERRPS)

T. Okanishi, K. Ohno, Yoshiaki Saito, 2009, Brain and Development.

Refractory epilepsy accompanying acute encephalitis with multifocal cortical lesions: Possible autoimmune etiology

K. Yokochi, T. Okanishi, Y. Maegaki, 2007, Brain and Development.

A case of congenital axonal neuropathy associated with West syndrome

I. Nonaka, M. Sasaki, E. Nakagawa, 2011, Brain and Development.

Effects of acetazolamide on epileptic apnea in migrating partial seizures in infancy

S. Nabatame, M. Sasaki, E. Nakagawa, 2011, Epilepsy Research.

Near-infrared Spectroscopy-based Assessment of Ictal Cerebral Hemodynamics of a Frontal Area in Startle Epilepsy

M. Sasaki, E. Nakagawa, K. Sugai, 2012 .

Startle epilepsy associated with gait‐induced seizures: Pathomechanism analysis using EEG, MEG, and PET studies

M. Sasaki, E. Nakagawa, Y. Kaneko, 2009, Epilepsia.

“Symptomatic” infection-associated acute encephalopathy in children with underlying neurological disorders

Y. Maegaki, Yoshiaki Saito, Yoshimichi Hirayama, 2017, Brain and Development.

MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene

Y. Goto, I. Nishino, M. Sasaki, 2014, Brain and Development.

Silicosis: expiratory thin-section CT assessment of airway obstruction.

P. Gevenois, V. De Maertelaer, Yoshiaki Saito, 2005, Radiology.

Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophy

A. Takahashi, K. Arima, M. Mizuguchi, 2009, Journal of the Neurological Sciences.

Brain MRI findings of older patients with Pallister–Killian syndrome

Y. Kuroki, K. Kurosawa, N. Aida, 2006, Brain and Development.

Computed tomography findings of Caplan syndrome.

Yoshiaki Saito, H. Morikubo, H. Arakawa, 2003, Journal of computer assisted tomography.

A review of functional and structural components of the respiratory center involved in the arousal response.

Yoshiaki Saito, Kayoko Saito, Makio Kobayashi, 2002, Sleep medicine.

Brainstem and spinal projections of augmenting expiratory neurons in the rat

K. Ezure, I. Tanaka, Yoshiaki Saito, 2003, Neuroscience Research.

Correlation of augmented startle reflex with brainstem electrophysiological responses in Tay–Sachs disease

M. Inagaki, M. Sasaki, K. Sugai, 2015, Brain and Development.

Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus

M. Iwasaki, K. Haginoya, S. Kure, 2016, Brain and Development.

Activity of Brainstem Respiratory Neurones just before the Expiration‐Inspiration Transition in the Rat

K. Ezure, I. Tanaka, Yoshiaki Saito, 2003, The Journal of physiology.

Difference between hypoglossal and phrenic activities during lung inflation and swallowing in the rat

K. Ezure, I. Tanaka, Yoshiaki Saito, 2002, The Journal of physiology.

Anterior striatum with dysmorphic neurons associated with the epileptogenesis of focal cortical dysplasia

A. Takahashi, A. Kakita, Hitoshi Takahashi, 2010, Seizure.

CD4+CD25high regulatory T cell in childhood ocular myasthenia gravis

M. Sasaki, E. Nakagawa, K. Sugai, 2011, Brain & development (Tokyo. 1979).

Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosis

I. Takamisawa, M. Sasaki, E. Nakagawa, 2012, Developmental medicine and child neurology.

Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study

A. Takahashi, M. Sasaki, E. Nakagawa, 2013, Brain and Development.

Characterization of ictal slow waves in epileptic spasms.

A. Okumura, M. Sasaki, E. Nakagawa, 2015, Epileptic disorders : international epilepsy journal with videotape.

IBA57 mutations abrogate iron-sulfur cluster assembly leading to cavitating leukoencephalopathy

Y. Goto, I. Nonaka, Y. Hayashi, 2017, Neurology: Genetics.

Low signal intensity and increased anisotropy on magnetic resonance imaging in the white matter lesion after head trauma: Unrecognized findings of diffuse axonal injury

S. Fujii, T. Okanishi, Y. Maegaki, 2007, Journal of the Neurological Sciences.

Focal cortical myoclonus in rolandic cortical dysplasia presenting as hemifacial twitching

A. Gunji, M. Sasaki, E. Nakagawa, 2012, Brain and Development.

Novel pathological abnormalities of deep brain structures including dysplastic neurons in anterior striatum associated with focal cortical dysplasia in epilepsy.

A. Takahashi, A. Kakita, Hitoshi Takahashi, 2012, Journal of neurosurgery. Pediatrics.

[Hereditary spastic paraplegia associated with congenital cataracts, mental retardation and peripheral neuropathy].

M. Sasaki, E. Nakagawa, K. Sugai, 2010, No to hattatsu = Brain and development.

Polysomnographic studies of Lesch–Nyhan syndrome

H. Morita, T. Hashimoto, M. Fukumizu, 1998, Brain and Development.

Surface electromyogram and muscle ultrasonography for detection of muscle fasciculations in pediatric peripheral neuropathy

I. Nishino, M. Oguri, Y. Maegaki, 2017, Brain and Development.

Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgery

A. Takahashi, Y. Nakata, M. Sasaki, 2014, Brain and Development.

Late‐onset, unusual neurological symptoms in children with mycoplasma infection

S. Kusunoki, Y. Maegaki, M. Shiota, 2009, Pediatrics International.

Pulmonary malignancy in silicosis: factors associated with radiographic detection.

N. Tomiyama, Mitsuko Tsubamoto, T. Johkoh, 2009, European journal of radiology.

Augmented startle responses in opsoclonus-myoclonus syndrome

T. Yonekawa, M. Inagaki, M. Sasaki, 2011, Brain & development (Tokyo. 1979).

Case report Augmented startle responses in opsoclonus-myoclonus syndrome

T. Yonekawa, M. Inagaki, M. Sasaki, 2011 .

[Long-term progression in a case of transvitreal endoresection of a posterior choroidal malignant melanoma].

K. Sugiyama, Yoshiaki Saito, M. Takahira, 2008, Nippon Ganka Gakkai zasshi.

Characteristics of Breathing Abnormality in Leigh and its Overlap Syndromes

M. Osawa, K. Nakano, Yoshiaki Saito, 2001, Neuropediatrics.

Hyperkinetic movement disorder in a child treated by globus pallidus stimulation

M. Sasaki, Hideyuki Nakama, T. Otsuki, 2009, Brain & development (Tokyo. 1979).

Importance of CAG repeat length in childhood-onset dentatorubral–pallidoluysian atrophy

Y. Goto, M. Sasaki, Hajime Tanaka, 2012, Journal of Neurology.

Hypoalbuminemia in early onset dentatorubral−pallidoluysian atrophy due to leakage of albumin in multiple organs

Y. Goto, S. Ito, K. Matsuoka, 2013, Journal of Neurology.

Congenital ocular motor apraxia: Clinical and neuroradiological findings, and long-term intellectual prognosis

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2007, Brain & development (Tokyo. 1979).

Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylation.

T. Okanishi, Y. Maegaki, I. Yuasa, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Forced mouth opening reaction: A primitive reflex released from cortical inhibition

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2006, Brain and Development.

Effects of phenobarbital, potassium bromide and topiramate on intractable epilepsies in two cases of holoprosencephaly

Yoshiaki Saito, M. Iwamoto, Keita Numasawa, 2023, Epilepsy & Seizure.

Frontotemporal abnormal gyration with infantile spasms in identical twins

Y. Maegaki, K. Ohno, Yoshiaki Saito, 2007, Brain and Development.

A patient with simplified gyral pattern followed by progressive brain atrophy

Y. Maegaki, M. Kuraoka, K. Ohno, 2007, Brain and Development.

Progressive diffuse brain atrophy in West syndrome with marked hypomyelination due to SPTAN1 gene mutation

N. Matsumoto, H. Saitsu, M. Ishii, 2013, Brain and Development.

Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phase

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