听力与言语-语言病理学

行为科学

医学伦理学

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  • Morvan syndrome following B-cell lymphoma.

    abstract::Morvan syndrome is a rare autoimmune disease named after the French physician Augustin Marie Morvan. It is characterized by multiple, irregular contractions of the long muscles, weakness, pruritus, hyperhidrosis, insomnia, and delirium. Here, we describe a 17-year-old young man, previously diagnosed with B-cell lympho...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809356108

    authors: El-Bitar MK,Muwakkit SA,Abboud MR,Sawaya RA,Boustany RM

    更新日期:2010-08-01 00:00:00

  • Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.

    abstract::A 14-year-old boy with an episode of acute weakness resembling acute demyelinating encephalomyelitis and polyradiculoneuritis after a febrile illness is described. Molecular analysis showed a mutation at codon 164 of the connexin 32 gene. Neuroradiological and neurophysiological follow-up is reported during acute and ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809344119

    authors: Fusco C,Frattini D,Pisani F,Spaggiari F,Ferlini A,Della Giustina E

    更新日期:2010-06-01 00:00:00

  • Long-term prognosis of pediatric patients with relapsing acute disseminated encephalomyelitis.

    abstract::Although long-term follow-up data are available for cases with acute disseminated encephalomyelitis, the findings range widely because of the lack of consistent definitions. Using the International Pediatric Multiple Sclerosis Study Group definitions strictly, we determined the long-term prognosis of children with acu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809343320

    authors: Mar S,Lenox J,Benzinger T,Brown S,Noetzel M

    更新日期:2010-06-01 00:00:00

  • Maternal methylenetetrahydrofolate reductase (MTHFR) homozygosity and neonatal outcome: follow-up of 42 pregnancies at risk.

    abstract::From February 2006 to March 2008, 42 pregnant women homozygous for the 677CT-methylenetetrahydrofolate reductase (MTHFR) allele were recruited in our obstetrics service for pregnancy at risk. All had antithrombotic prophylaxis with low-dose aspirin and/or low-molecular-weight heparin, supplemented with folic acid. In ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809344622

    authors: Pogliani L,Muggiasca L,Arrigoni L,Rossi E,Zuccotti G

    更新日期:2010-06-01 00:00:00

  • Impact of bacille Calmette-Guérin vaccination on neuroradiological manifestations of pediatric tuberculous meningitis.

    abstract::The authors conducted this study to identify whether bacille Calmette-Guérin (BCG) vaccination leads to an altered spectrum of neuroimaging findings outcome in pediatric patients with tuberculous meningitis. This retrospective study was conducted through chart review and review of computed tomography (CT) scans and ma...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809340921

    authors: Wasay M,Ajmal S,Taqui AM,Uddin N,Azam I,Husen Y,Nizami SQ

    更新日期:2010-05-01 00:00:00

  • Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.

    abstract::CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a progressive neurodegenerative condition, associated with mutations in the notch3 gene. Symptoms include migraine with aura, mood disorders, progressive cognitive decline, subcortical ischemic strokes, dementia, an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810361382

    authors: Hartley J,Westmacott R,Decker J,Shroff M,Yoon G

    更新日期:2010-05-01 00:00:00

  • Electroencephalogram discharges in atypical cognitive development.

    abstract::To investigate the significance of electroencephalogram (EEG) discharges and their treatment, we retrospectively reviewed the charts of 22 children with atypical cognitive development that did not respond to standard educational therapy and demonstrated discharges on EEG. Most children demonstrated no obvious symptoms...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809344743

    authors: Frye RE,Butler I,Strickland D,Castillo E,Papanicolaou A

    更新日期:2010-05-01 00:00:00

  • Child neurology practice and neurological disorders in East Africa.

    abstract::Neurological disorders, including neurodevelopmental disorders, have been identified by the World Health Organization (WHO) as one of the greatest threats to global public health. It is generally believed that these conditions are more prevalent in the developing than the developed world because of multiple known risk...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073809357792

    authors: Idro R,Newton C,Kiguli S,Kakooza-Mwesige A

    更新日期:2010-04-01 00:00:00

  • Klebsiella pneumoniae brain abscess in neonates: a report of 2 cases.

    abstract::Brain abscesses are uncommon in neonates. Klebsiella pneumoniae is a very uncommon microbial agent to cause brain abscess. We report 2 infants with Klebsiella pneumoniae sepsis who developed brain abscesses. One infant was a premature neonate who required mechanical ventilation for respiratory distress syndrome and su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809338326

    authors: Sundaram V,Agrawal S,Chacham S,Mukhopadhyay K,Dutta S,Kumar P

    更新日期:2010-03-01 00:00:00

  • From apneic spells to the development of hypertensive hydrocephalus: a case report of homocystinuria with early onset.

    abstract::Homocystinuria represents a group of hereditary metabolic disorders characterized by an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine. The infantile form is severe: the main clinical findings are neurologic signs, associated with hematological signs and bone alterati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809336877

    authors: Cerbo RM,Cabano R,Lombardi G,Bollani L,Colombo R,Stronati M

    更新日期:2010-03-01 00:00:00

  • Psychiatric comorbidity in pediatric patients with demyelinating disorders.

    abstract::Little is known about psychiatric aspects of pediatric demyelinating conditions. A total of 23 youths (6-17 years) with demyelinating conditions underwent semistructured psychiatric interviews using the Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version. Adolescents...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809338519

    authors: Weisbrot DM,Ettinger AB,Gadow KD,Belman AL,MacAllister WS,Milazzo M,Reed ML,Serrano D,Krupp LB

    更新日期:2010-02-01 00:00:00

  • Paramyotonia congenita in 22 members of an Arab (Omani) kindred.

    abstract::Paramyotonia congenita in 22 members of Arab (Omani) family is reported. Four generations were affected. All had early onset around 1 year of age, with myotonia and cold intolerance. Age of onset in the index case was at 3 months of age. Six members with the disease were examined and investigated. To our knowledge, th...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808330185

    authors: Koul R,Alfutaisi A,Hira M

    更新日期:2010-02-01 00:00:00

  • Meralgia paresthetica in the pediatric population: a propos of 2 cases.

    abstract::Meralgia paresthetica is a mononeuropathy affecting the lateral femoral cutaneous nerve that is extremely rare in children. Two adolescent females, aged 11 and 13 years, presented due to tingling and pain on the side of the thigh of 2 to 3 weeks duration. The general examination revealed mild obesity; the neurological...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809336130

    authors: Fernández-Mayoralas DM,Fernández-Jaén A,Jareño NM,Pérez BC,Fernández PM,Sola AG

    更新日期:2010-01-01 00:00:00

  • Practice parameters in child neurology: do pediatricians use them?

    abstract::We assessed pediatrician awareness of the parameter ''Evaluating the first non-febrile seizure in children'' and how the concepts of this parameter were incorporated into practice. Although most reported caring for children with seizures, 60% were not aware of the practice parameter. When given the clinical scenario o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809332766

    authors: Bale JF Jr,Caplin DA,Bruse JD,Folland D

    更新日期:2009-12-01 00:00:00

  • Reversible coma associated with prolonged high-dose phenobarbital therapy in bilateral Sturge-Weber syndrome.

    abstract::High-dose phenobarbital therapy is an effective treatment for refractory status epilepticus in children. The advantages of this therapy include milder adverse effects without limits for maximal phenobarbital levels or doses during the initial phase of treatment. However, little is known about the safety of continuing ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331360

    authors: Wakamoto H,Nakamura Y,Ebihara T,Tokuda K,Ohmori H

    更新日期:2009-12-01 00:00:00

  • Ependymoma: an update.

    abstract::The authors provide an update on most issues related to biology, diagnosis, and treatment of children with ependymoma based on a literature review. Ependymoma is the third most common brain tumor in children and overall survival ranges from 24% to 75% at 5 years. The extent of surgical resection remains the principal ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073809339212

    authors: Zacharoulis S,Moreno L

    更新日期:2009-11-01 00:00:00

  • Intrauterine endotoxin administration leads to white matter diffusivity changes in newborn rabbits.

    abstract::Maternal intrauterine inflammation has been implicated in the development of periventricular leukomalacia and white matter injury in the neonate. We hypothesized that intrauterine endotoxin administration would lead to microstructural changes in the neonatal rabbit white matter in vivo that could be detected at birth ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809338213

    authors: Saadani-Makki F,Kannan S,Makki M,Muzik O,Janisse J,Romero R,Chugani D

    更新日期:2009-09-01 00:00:00

  • Parent-based sleep education workshops in autism.

    abstract::To determine if parents can successfully teach their children with autism spectrum disorders to become better sleepers, we piloted small group parent education workshops focused on behavioral sleep strategies. Workshops consisted of three 2-hour sessions conducted over consecutive weeks by 2 physicians. Curricula incl...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331348

    authors: Reed HE,McGrew SG,Artibee K,Surdkya K,Goldman SE,Frank K,Wang L,Malow BA

    更新日期:2009-08-01 00:00:00

  • Managing severe epilepsy syndromes of early childhood.

    abstract::Managing severe epilepsy syndromes of early childhood is challenging as the seizures are typically resistant to treatment and may cause disabling mental and behavioral problems in later life. A comprehensive treatment plan includes pharmacologic, nonpharmacologic, and surgical options. This article reviews clinical st...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073809338153

    authors: Wheless JW

    更新日期:2009-08-01 00:00:00

  • Acute disseminated encephalomyelitis with bilateral thalamic necrosis.

    abstract::Acute disseminated encephalomyelitis is a monophasic inflammatory demyelinating disease of the central nervous system involving the white matter, and to a lesser extent, the gray matter. Bilateral thalamic lesions have been reported in 12% of pediatric patients with acute disseminated encephalomyelitis. In most cases,...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331364

    authors: Dardiotis E,Kountra P,Kapsalaki E,Protogerou G,Markopoulou K

    更新日期:2009-08-01 00:00:00

  • Growth patterns in children with intrauterine growth retardation and their correlation to neurocognitive development.

    abstract::The relationship between somatic growth and neurocognitive outcome was studied in a cohort of 136 children with intrauterine growth retardation. The children were followed up from birth to 9 to 10 years of age by annual measurements of growth parameters, neurodevelopmental evaluations, and IQ. The rate of catch-up for...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331082

    authors: Fattal-Valevski A,Toledano-Alhadef H,Leitner Y,Geva R,Eshel R,Harel S

    更新日期:2009-07-01 00:00:00

  • Subacute sclerosing panencephalitis (SSPE) presenting as acute disseminated encephalomyelitis in a child.

    abstract::Subacute sclerosing panencephalitis (SSPE) typically presents with progressive mental deterioration, behavioral changes, and myoclonic jerks. Atypical presentations are not unknown and may result in diagnostic delays. A 9-year-old girl presented with poor balance and ataxia following an episode of upper respiratory tr...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808330184

    authors: Goraya J,Marks H,Khurana D,Legido A,Melvin J

    更新日期:2009-07-01 00:00:00

  • Unilateral palatal and abducens palsy in childhood hepatitis A virus infection.

    abstract::Isolated cranial nerve paresis in childhood hepatitis A virus infection is rare. The authors report an instance of concomitant right-hand side palatal and abducens palsy, developing in the course of an otherwise uncomplicated hepatitis A virus infection in a 5-year-old girl. The neurological complications were transie...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808323026

    authors: Thapa R,Biswas B,Ghosh A,Mukherjee S

    更新日期:2009-05-01 00:00:00

  • Stimulus-induced diffuse voltage attenuation (SIDVA): a previously undescribed EEG pattern in a critically ill child.

    abstract::We report the case of a 15-month-old critically ill child with stimulus-induced diffuse voltage attenuation, a previously unreported electroencephalogram pattern. No clinical evidence of seizure activity was associated with these EEG changes. The patient went on to have a full recovery. This case suggests that critica...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808324532

    authors: Losey TE,Ng YT

    更新日期:2009-04-01 00:00:00

  • Phenotypic variations in 3 children with POLG1 mutations.

    abstract::Autosomal inherited mitochondrial diseases have been of increasing interest among clinicians and mitochondrial research groups because these diseases are caused through a secondary effect on the mitochondrial DNA. It was thought that the genetic stability of mitochondrial DNA relies on the accuracy of DNA polymerase g...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808324539

    authors: Burusnukul P,de los Reyes EC

    更新日期:2009-04-01 00:00:00

  • Insights on chronic-relapsing opsoclonus-myoclonus from a pilot study of mycophenolate mofetil.

    abstract::Opsoclonus-myoclonus syndrome is characterized by abnormal lymphocyte trafficking into brain. The authors hypothesized that mycophenolate mofetil, a lymphocyte proliferation inhibitor, might be therapeutic. The cerebrospinal fluid and blood immunophenotypes of 15 children with predominantly chronic-relapsing opsoclonu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808324217

    authors: Pranzatelli MR,Tate ED,Travelstead AL,Baumgardner CA,Gowda NV,Halthore SN,Kerstan P,Kossak BD,Mitchell WG,Taub JW

    更新日期:2009-03-01 00:00:00

  • Successful treatment of cytomegalovirus polyradiculopathy in a 9-year-old child with congenital human immunodeficiency virus infection.

    abstract::Cytomegalovirus lumbosacral polyradiculopathy is a well-documented complication of human immunodeficiency virus in adults who have a CD4 count of less than 40/microL. Patients present with an acute ascending flaccid paralysis of the lower limbs with areflexia, paresthesia, and urinary and bowel symptoms. However, it a...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808322671

    authors: Sohal A,Riordan A,Mallewa M,Solomon T,Kneen R

    更新日期:2009-02-01 00:00:00

  • Neonatal seizures: treatment and treatment variability in 31 United States pediatric hospitals.

    abstract::Neonatal seizures are one of the most common neurological disorders in infants. However, the optimal treatment strategy for neonatal seizures remains controversial and there is little data regarding current treatment of neonatal seizures. In this study we describe the current treatment of neonatal seizures and variati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808321056

    authors: Blume HK,Garrison MM,Christakis DA

    更新日期:2009-02-01 00:00:00

  • Serum and muscle carnitine levels in epileptic children receiving sodium valproate.

    abstract::The purpose of this study was to determine whether children with epilepsy undergoing valproate therapy and who are otherwise healthy have lower levels of serum and muscle carnitine. A total of 50 patients with epilepsy, 3 to 14 years of age, who were treated solely with valproate and free of abnormal neurologic findin...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/0883073808321060

    authors: Anil M,Helvaci M,Ozbal E,Kalenderer O,Anil AB,Dilek M

    更新日期:2009-01-01 00:00:00

  • Pyridoxine-dependent seizures caused by alpha amino adipic semialdehyde dehydrogenase deficiency: the first polish case with confirmed biochemical and molecular pathology.

    abstract::Pyridoxine-dependent seizures are a rare condition recognized when numerous seizures respond to pyridoxine treatment and recur on pyridoxine withdrawal. For decades the diagnosis was confirmed only with pyridoxine treatment withdrawal trial. Recently described biochemical and molecular pathology improved the diagnosti...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808318543

    authors: Kaczorowska M,Kmiec T,Jakobs C,Kacinski M,Kroczka S,Salomons GS,Struys EA,Jozwiak S

    更新日期:2008-12-01 00:00:00

  • Atypical teratoid/rhabdoid tumor of the spine in a 4-year-old girl.

    abstract::Primary spinal atypical teratoid/rhabdoid tumor is extremely rare. The authors present a case of atypical teratoid/rhabdoid tumor occurring in a 4-year-old girl. Magnetic resonance imaging The authors showed an intramedullary mass extending from the bulbomedullary junction to T1 with leptomeningeal dissemination. The ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808319319

    authors: Tinsa F,Jallouli M,Douira W,Boubaker A,Kchir N,Hassine DB,Boussetta K,Bousnina S

    更新日期:2008-12-01 00:00:00

  • Juvenile dermatomyositis presenting with anasarca.

    abstract::Generalized edema can occur during the course of juvenile dermatomyositis. In this article, a 4-year-old boy with generalized nonpitting edema and proximal weakness is reported. Characteristic cutaneous lesions, laboratory tests, results of electromyography, and magnetic resonance imaging findings resulted in a diagno...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808318544

    authors: Saygi S,Alehan F,Baskin E,Bayrakci US,Ulu EM,Ozbek N

    更新日期:2008-11-01 00:00:00

  • High-dose riboflavin for migraine prophylaxis in children: a double-blind, randomized, placebo-controlled trial.

    abstract::This is the first study to evaluate the efficacy of riboflavin for migraine prophylaxis in children. This was a randomized, double-blind study of riboflavin (200 mg daily) versus placebo in 48 children. The primary efficacy measure was the number of patients achieving a 50% or greater reduction in the number of migrai...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1177/0883073808318053

    authors: MacLennan SC,Wade FM,Forrest KM,Ratanayake PD,Fagan E,Antony J

    更新日期:2008-11-01 00:00:00

  • Leucoencephalopathy, transverse myelopathy, and peripheral neuropathy in association with glutamic acid decarboxylase-65 (GAD) antibodies in children with cancer.

    abstract::Neurologic toxicity may occur as a direct effect of cancer and its therapy or indirectly because of a dysfunctional immune system. The authors report the development of axonal neuropathy, myelopathy, and leucoencephalopathy associated with glutamic acid decarboxylase-65 (GAD) antibodies in 4 children with progressive ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808315617

    authors: Ledet DS,Handgretinger R,Bertorini TE,Hale GA,Ribeiro RC,Khan RB

    更新日期:2008-11-01 00:00:00

  • Convection-enhanced delivery for the treatment of pediatric neurologic disorders.

    abstract::Direct perfusion of specific regions of the central nervous system by convection-enhanced delivery is becoming more widely used for the delivery of compounds in the research and treatment of various neural disorders. In contrast to other currently available central nervous system delivery techniques, convection-enhanc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073808321064

    authors: Song DK,Lonser RR

    更新日期:2008-10-01 00:00:00

  • Initial management of childhood brain tumors: neurosurgical considerations.

    abstract::Intracranial tumors are the most common solid tumors in children. The infratentorial compartment will be the primary site for 60% to 70% of these tumors, including astrocytomas, medulloblastomas, and ependymomas. Several technological advancements have increased our knowledge of the cell biology of pediatric brain tum...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073808321768

    authors: Nejat F,El Khashab M,Rutka JT

    更新日期:2008-10-01 00:00:00

  • Divergent ependymal tumor (ependymoblastoma/anaplastic ependymoma) of the posterior fossa: an uncommon case observed in a child.

    abstract::We report a divergent ependymal tumor of the posterior fossa (ependymoblastoma/anaplastic ependymoma) observed in an 8-year-old boy. The tumor showed the histological pattern typical of an ependymoblastoma (tubular-papillary fetaloid architecture with stratification of the tumor cells) next to areas in which findings ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314160

    authors: Ortiz J,Otero A,Bengoechea O,Gonçalves J,Sousa P,Figols J,Bullón A

    更新日期:2008-09-01 00:00:00

  • Hypnagogic behavior disorder: complex motor behaviors during wake-sleep transitions in 2 young children.

    abstract::A nondescribed behavioral disorder was observed during wake-sleep transitions in 2 young children. Two boys had episodes of abnormal behavior in hypnagogic-and occasionally hypnopompic-periods for 1 year from the time they were 1 year and several months old. The episodes consisted of irregular body movements, which co...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314964

    authors: Pareja JA,Cuadrado ML,García-Morales I,Gil-Nagel A,Franch O

    更新日期:2008-08-01 00:00:00

  • Learning disabilities spectrum and sexual dimorphic abilities in girls with congenital adrenal hyperplasia.

    abstract::Congenital adrenal hyperplasia could provide a promising model for the study of the effects of hormones on cognition. The aim of this study was to assess sexual dimorphic abilities related to oral language, spatial abilities, and verbal fluency and to determine the existence of learning disabilities in 11 congenital g...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808315618

    authors: Inozemtseva O,Matute E,Juárez J

    更新日期:2008-08-01 00:00:00

  • Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.

    abstract::Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease characterized by early-onset and slowly progressive cerebellar ataxia, areflexia, and peripheral neuropathy. Ocular apraxia is most prominent in the early stage of the disease, by contrast, hypoalbuminemia, hypercholesterolemia, and cogniti...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314959

    authors: D'Arrigo S,Riva D,Bulgheroni S,Chiapparini L,Castellotti B,Gellera C,Pantaleoni C

    更新日期:2008-08-01 00:00:00

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