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La ricerca find articoli where soggetti phrase all words 'developmental delay' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 191 riferimenti
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    1. Wang, YH; Korman, SH; Ye, J; Gargus, JJ; Gutman, A; Taroni, F; Garavaglia, B; Longo, N
      Phenotype and genotype variation in primary carnitine deficiency

      GENETICS IN MEDICINE
    2. Fan, YS; Zhang, Y; Speevak, M; Farrell, S; Jung, JH; Siu, VM
      Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes

      GENETICS IN MEDICINE
    3. Jacobson, JW
      Environmental postmodernism and rehabilitation of the borderline of mentalretardation

      BEHAVIORAL INTERVENTIONS
    4. Skellern, CY; Rogers, Y; O'Callaghan, MJ
      A parent-completed developmental questionnaire: Follow up of ex-premature infants

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    5. Thai, TP; Rodemer, C; Jauch, A; Hunziker, A; Moser, A; Gorgas, K; Just, WW
      Impaired membrane traffic in defective ether lipid biosynthesis

      HUMAN MOLECULAR GENETICS
    6. Iwata, T; Li, CL; Deng, CX; Francomano, CA
      Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice

      HUMAN MOLECULAR GENETICS
    7. Lemire, EG; Stoeber, GP; Anselmo, M; Lowry, RB
      Two brothers with severe developmental delay, growth retardation and unusual appearance

      CLINICAL DYSMORPHOLOGY
    8. de Vries, BBA; van't Hoff, WG; Surtees, RAH; Winter, RM
      Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay

      CLINICAL DYSMORPHOLOGY
    9. Bailey, DB; Roberts, JE; Mirrett, P; Hatton, DD
      Identifying infants and toddlers with fragile X syndrome: Issues and recommendations

      INFANTS AND YOUNG CHILDREN
    10. Buck, DM; Cox, AW; Shannon, P; Hash, K
      Building collaboration among physicians and other early intervention providers: Practices that work

      INFANTS AND YOUNG CHILDREN
    11. Astington, JW; Barriault, T
      Children's theory of mind: How young children come to understand that people have thoughts and feelings

      INFANTS AND YOUNG CHILDREN
    12. Shevell, MI; Majnemer, A; Rosenbaum, P; Abrahamowicz, M
      Etiologic yield of autistic spectrum disorders: A prospective study

      JOURNAL OF CHILD NEUROLOGY
    13. Shevell, MI; Majnemer, A; Rosenbaum, P; Abrahamowicz, M
      Etiologic determination of childhood developmental delay

      BRAIN & DEVELOPMENT
    14. Noffke, AS; Feder, RS; Greenwald, MJ; O'Grady, RB; Roth, SI
      Mucolipidosis IV in an African American patient with new findings on electron microscopy

      CORNEA
    15. Stein, MT; Dixon, S; Cowan, C
      A two-year-old boy with language regression and unusual social interactions

      JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
    16. Adamson, LB; McArthur, D; Markov, Y; Dunbar, B; Bakeman, R
      Autism and joint attention: Young children's responses to maternal bids

      JOURNAL OF APPLIED DEVELOPMENTAL PSYCHOLOGY
    17. Williams, E; Reddy, V; Costall, A
      Taking a closer look at functional play in children with autism

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    18. Morrissette, JJD; Celle, L; Owens, NL; Shields, CL; Zackai, EH; Spinner, NB
      Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Kumada, S; Hayashi, M; Kenmochi, J; Kurosawa, S; Shimozawa, N; Kratz, LE; Kelley, RI; Taki, K; Okaniwa, M
      Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Schweitzer, DN; Graham, JM; Lachman, RS; Jabs, EW; Okajima, K; Przylepa, KA; Shanske, A; Chen, K; Neidich, JA; Wilcox, WR
      Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Torrisi, L; Sangiorgi, E; Russo, L; Gurrieri, F
      Rearrangements of chromosome 15 in epilepsy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    22. Bolton, PF; Dennis, NR; Browne, CE; Thomas, NS; Veltman, MWM; Thompson, RJ; Jacobs, P
      The phenotypic manifestations of interstitial duplications of proximal 15qwith special reference to the autistic spectrum disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Fang, LJ; Chalhoub, N; Li, WT; Feingold, J; Ortenberg, J; Lemieux, B; Thirion, JP
      Genotype analysis of the NF1 gene in the French Canadians from the Quebec population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Ng, D; Mowrey, P; Ragoussis, J; Mirza, G; Coll, E; Di Fazio, MP; Turner, C; Levin, SW
      Molecularly defined interstitial tandem duplication 6p case with mild manifestations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Fan, YS; Siu, VM; Jung, JH; Farrell, SA; Cote, GB
      Direct duplication of 8p21.3 -> p23.1: A cytogenetic anomaly associated with developmental delay without consistent clinical features

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Roscioli, T; Flanagan, S; Mortimore, RJ; Kumar, P; Weedon, D; Masel, J; Lewandowski, R; Hyland, V; Glass, IA
      Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Phelan, MC; Rogers, RC; Saul, RA; Stapleton, GA; Sweet, K; McDermid, H; Shaw, SR; Claytor, J; Willis, J; Kelly, DP
      22q13 deletion syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Bacha, F; Hoo, JJ
      New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Rudnick, E; Khakoo, Y; Antunes, NL; Seeger, RC; Brodeur, GM; Shimada, H; Gerbing, RB; Stram, DO; Matthay, KK
      Opsoclonus-myoclonus-ataxia syndrome in neuroblastoma: Clinical outcome and antineuronal antibodies - A report from the Children's Cancer Group study

      MEDICAL AND PEDIATRIC ONCOLOGY
    30. Stein, MT; Cowan, C; Dixon, S
      A two-year-old boy with language regression and unusual social interactions

      PEDIATRICS
    31. Edery, P; Le Deist, F; Briard, ML; Debre, M; Munnich, A; Griscelli, C; Fischer, A; Lyonnet, S
      B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

      JOURNAL OF MEDICAL GENETICS
    32. Ungaro, P; Christian, SL; Fantes, JA; Mutirangura, A; Black, S; Reynolds, J; Malcolm, S; Dobyns, WB; Ledbetter, DH
      Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14

      JOURNAL OF MEDICAL GENETICS
    33. Pisecco, S; Baker, DB; Silva, PA; Brooke, M
      Boys with reading disabilities and/or ADHD: Distinctions in early childhood

      JOURNAL OF LEARNING DISABILITIES
    34. Croft, C; O'Connor, TG; Keaveney, L; Groothues, C; Rutter, M
      Longitudinal change in parenting associated with developmental delay and catch-up

      JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
    35. Anderson, M
      Annotation: Conceptions of intelligence

      JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
    36. Imamura, Y; Kondoh, T; Kamei, T; Tsuru, A; Shimasaki, Y; Kinoshita, E; Matsumoto, T; Moriuchi, H
      A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia

      PEDIATRICS INTERNATIONAL
    37. Mao, R; Jalal, SM; Snow, K; Michels, VV; Szabo, SM; Babovic-Vuksanovic, D
      Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin

      GENETICS IN MEDICINE
    38. Calandrella, AM; Wilcox, MJ
      Predicting language outcomes for young prelinguistic children with developmental delay

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    39. Westall, CA; Ainsworth, JR; Buncic, JR
      Which ocular and neurologic conditions cause disparate results in visual acuity scores recorded with visually evoked potential and teller acuity cards?

      JOURNAL OF AAPOS
    40. Wang, D; Kranz-Eble, P; De Vivo, DC
      Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome

      HUMAN MUTATION
    41. Bal, M; Schrander-Stumpel, CTRM; Meers, LEC; Theunissen, PMVM; Hamers, AJH; Wennekes, MJ; Engelen, JJM
      De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism

      GENETIC COUNSELING
    42. Stewart, H; Kerr, B; Tomlin, P; Stacey, D; Super, M
      Sibs with developmental delay, hirsutism and nail hypoplasia: a new syndrome

      CLINICAL DYSMORPHOLOGY
    43. Rajab, A; Riaz, A; Paul, G; Al-Khusaibi, S; Chalmers, R; Patton, MA
      Further delineation of the DOOR syndrome

      CLINICAL DYSMORPHOLOGY
    44. Priolo, M; Lerone, M; Rosaia, L; Calcagno, EP; Sadeghi, AK; Ghezzi, F; Ravazzolo, R; Silengo, M
      Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?

      CLINICAL DYSMORPHOLOGY
    45. Kristensen, H
      Selective mutism and comorbidity with developmental disorder/delay, anxiety disorder, and elimination disorder

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    46. Jenne, DE; Tinschert, S; Stegmann, E; Reimann, H; Nurnberg, P; Horn, D; Naumann, I; Buske, A; Thiel, G
      A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions

      GENOMICS
    47. Goizet, C; Excoffier, E; Taine, L; Taupiac, E; El Moneim, AA; Arveiler, B; Bouvard, M; Lacombe, D
      Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Gropman, A; Levin, S; Yao, L; Lin, T; Suchy, S; Sabnis, S; Hadley, D; Nussbaum, R
      Unusual renal features of Lowe syndrome in a mildly affected boy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Gohlich-Ratmann, G; Lackner, A; Schaper, J; Voit, T; Gillessen-Kaesbach, G
      Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: Specific entity or variant of a described condition?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Hussain, SZ; Evans, AL; Ahmed, OA; Jones, D; McDermot, KD; Svennevik, EC; Hastings, RJ
      Non-syndromic mental retardation segregating with an apparently balanced t(1;17) reciprocal translocation through three generations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Blair, EM; Walsh, S; Oldridge, M; Wall, SS; Wilkie, AOM
      Newly recognised craniosynostosis syndrome that does not map to known disease loci

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Amor, DJ; Leventer, RJ; Hayllar, S; Bankier, A
      Polymicrogyria associated with scalp and limb defects: Variant of Adams-Oliver syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. Smith, RL; Edwards, MJ; Notaras, E; O'Loughlin, EV
      Esophageal dysmotility in brothers with an FG-like syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Scaglia, F; Bodamer, OAF; Berend, SA; Adam, LR; Shaffer, LG
      Deletion (9) (p13.1 p21.1)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. Moore, C; Adler, R
      Herbal vitamins: Lead toxicity and developmental delay

      PEDIATRICS
    56. Miller, RI; Clarren, SK
      Long-term developmental outcomes in patients with deformational plagiocephaly

      PEDIATRICS
    57. Robertson, SP; Rodda, C; Bankier, A
      Hypogonadotrophic hypogonadism in Roifman syndrome

      CLINICAL GENETICS
    58. Glass, IA; Trenholme, A; Mildenhall, L; Bailey, RJ; Cotter, PD
      Mild phenotype in two siblings with distal monosomy 12p13.31 -> pter

      CLINICAL GENETICS
    59. Prasad, C; Prasad, AN; Chodirker, BN; Lee, C; Dawson, AK; Jocelyn, LJ; Chudley, AE
      Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

      CLINICAL GENETICS
    60. Agustines, LA; Lin, YG; Rumney, PJ; Lu, MC; Bonebrake, R; Asrat, T; Nageotte, M
      Outcomes of extremely low-birth-weight infants between 500 and 750 g

      AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
    61. Bellus, GA; Spector, EB; Speiser, PW; Weaver, CA; Garber, AT; Bryke, CR; Israel, J; Rosengren, SS; Webster, MK; Donoghue, DJ; Francomano, CA
      Distinct missense mutations of the FCFR3 Lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype

      AMERICAN JOURNAL OF HUMAN GENETICS
    62. Riva, P; Corrado, L; Natacci, F; Castorina, P; Wu, BL; Schneider, GH; Clementi, M; Tenconi, R; Korf, BR; Larizza, L
      NF1 microdeletion syndrome: Refined FISH characterization of sporadic and familial deletions with locus-specific probes

      AMERICAN JOURNAL OF HUMAN GENETICS
    63. Ko, TS; Holmes, GL
      EEG and clinical predictors of medically intractable childhood epilepsy

      CLINICAL NEUROPHYSIOLOGY
    64. McCathren, RB; Yoder, PJ; Warren, SF
      The relationship between prelinguistic vocalization and later expressive vocabulary in young children with developmental delay

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    65. Mccathren, RB; Yoder, PJ; Warren, SF
      Prelinguistic pragmatic functions as predictors of later expressive vocabulary

      JOURNAL OF EARLY INTERVENTION
    66. Frisk, M
      A complex background in children and adolescents with psychiatric disorders: Developmental delay, dyslexia, heredity, slow cognitive processing and adverse social factors in a multifactorial entirety

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    67. Christian, SL; Fantes, JA; Mewborn, SK; Huang, B; Ledbetter, DH
      Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)

      HUMAN MOLECULAR GENETICS
    68. Kreuz, FR; Nolte-Buchholtz, S; Fackler, F; Behrens, R
      Another case of achalasia-microcephaly syndrome

      CLINICAL DYSMORPHOLOGY
    69. Fanurik, D; Koh, JL; Schmitz, ML; Harrison, RD; Roberson, PK; Killebrew, P
      Pain assessment and treatment in children with cognitive impairment: A survey of nurses' and physicians' beliefs

      CLINICAL JOURNAL OF PAIN
    70. Talkop, UA; Klaassen, T; Piirsoo, A; Sander, V; Napa, A; Essenson, E; Tammur, J; Talvik, T
      Duchenne and Becker muscular dystrophies: an Estonian experience

      BRAIN & DEVELOPMENT
    71. Grindel, SI; Sandlin, C; Wood, VE
      Hand involvement in 13q deletion syndrome

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    72. Williams, E; Costall, A; Reddy, V
      Children with autism experience problems with both objects and people

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    73. Carey, JC; Viskochil, DH
      Neurofibromatosis type 1: A model condition for the study of the molecularbasis of variable expressivity in human disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Magenis, E; Webb, MJ; Spears, B; Opitz, JM
      Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism

      AMERICAN JOURNAL OF MEDICAL GENETICS
    75. Lemire, EG; Cardwell, S
      Unusual phenotype in partial trisomy 14

      AMERICAN JOURNAL OF MEDICAL GENETICS
    76. Streubel, B; Latta, E; Kehrer-Sawatzki, H; Hoffmann, GF; Fonatsch, C; Rehder, H
      Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: Further evidence for a contiguous gene syndrome in 17q11.2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    77. Horelli-Kuitunen, N; Gahmberg, N; Eeva, M; Palotie, A; Jarvela, I
      Interstitial deletion of bands 11q21 -> 22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    78. Achermann, S; Largo, R; Kotzot, D; Riegel, M; Schinzel, A
      Short stature, myopia, severe developmental delay, and peculiar facial appearance in two brothers: A new syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    79. Sreekantaiah, C; Kronn, D; Marinescu, RC; Goldin, B; Overhauser, J
      Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. del Campo, M; Hall, BD; Aeby, A; Nassogne, MC; Verloes, A; Roche, C; Gonzalez, C; Sanchez, H; Garcia-Alix, A; Cabanas, F; Escudero, RM; Hernandez, R; Quero, J
      Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. Diaz, GA; Gelb, BD; Ali, F; Sakati, N; Sanjad, S; Meyer, BF; Kambouris, M
      Sanjad-sakati and autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement

      AMERICAN JOURNAL OF MEDICAL GENETICS
    82. Schutte, BC; Basart, AM; Watanabe, Y; Laffin, JJS; Coppage, K; Bjork, BC; Daack-Hirsch, S; Patil, S; Dixon, MJ; Murray, JC
      Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    83. Meyers, KEC; Kaplan, P; Kaplan, BS
      Nephrotic syndrome, microcephaly, and developmental delay: Three separate syndromes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Battaglia, A; Bianchini, E; Carey, JC
      Diagnostic yield of the comprehensive assessment of developmental delay mental retardation in an institute of child neuropsychiatry

      AMERICAN JOURNAL OF MEDICAL GENETICS
    85. Doty, AK; McEwen, IR; Parker, D; Laskin, J
      Effects of testing context on ball skill performance in 5-year-old children with and without developmental delay

      PHYSICAL THERAPY
    86. Turner, M
      Annotation: Repetitive behaviour in autism: A review of psychological research

      JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
    87. Tang, Q; Rice, DS; Goldowitz, D
      Disrupted retinal development in the embryonic belly spot and tail mutant mouse

      DEVELOPMENTAL BIOLOGY
    88. Dean, JCS; Moore, SJ; Osborne, A; Howe, J; Turnpenny, PD
      Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene

      CLINICAL GENETICS
    89. Sabry, MA; Farag, TI; Shaltout, AA; Zaki, M; Al-Mazidi, Z; Abulhassan, SJ; Al-Torki, N; Quishawi, A; Al Awadi, SA
      Kenny-Caffey syndrome: an Arab variant?

      CLINICAL GENETICS
    90. Hill, SY; Shen, S; Locke, J; Steinhauer, SR; Konicky, C; Lowers, L; Connolly, J
      Developmental delay in P300 production in children at high risk for developing alcohol-related disorders

      BIOLOGICAL PSYCHIATRY
    91. Oda, N; Abe, K
      Sex differences in children with developmental speech delay: A follow-up study

      RECENT PROGRESS IN CHILD AND ADOLESCENT PSYCHIATRY, VOL 2
    92. SCHROEDER CM; SCHUSTER JW; HEMMETER ML
      EFFICIENCY IN PROGRAMMING FOR GENERALIZATION - COMPARISON OF 2 METHODS FOR TEACHING EXPRESSIVE LABELING TO PRESCHOOLERS WITH DEVELOPMENTAL DELAYS

      Journal of developmental and physical disabilities
    93. LEVENTER RJ; HARVEY AS
      CORTICAL MALFORMATIONS - A SIGNIFICANT CAUSE OF PEDIATRIC NEUROLOGICAL MORBIDITY

      Journal of paediatrics and child health
    94. WHEELER PG; MEDINA S; DUSICK A; BULL MJ; ANDREOLI SP; EDWARDSBROWN M; WEAVER DD
      LIVEDO-RETICULARIS, DEVELOPMENTAL DELAY AND STROKE-LIKE EPISODE IN A 7-YEAR-OLD MALE

      Clinical dysmorphology
    95. HERGE EA; CAMPBELL JE
      THE ROLE OF THE OCCUPATIONAL AND PHYSICAL THERAPIST IN THE REHABILITATION OF THE OLDER ADULT WITH MENTAL-RETARDATION

      Topics in geriatric rehabilitation
    96. TANAKA H
      FETAL ALCOHOL SYNDROME - A JAPANESE PERSPECTIVE

      Annals of medicine
    97. PARK ES; PARK CI; LEE JK; YIM SY
      CORRELATION OF BRAIN CT FINDINGS AND DEVELOPMENTAL OUTCOME IN PATIENTS WITH SPASTIC CEREBRAL-PALSY

      Yonsei medical journal
    98. ALANSARI SS; BELLA H
      NORMAL DEVELOPMENTAL MILESTONES - COMPARISON OF URBAN AND RURAL CHILDREN IN MADINAH, SAUDI-ARABIA

      Saudi medical journal
    99. GLAUN DE; COLE KE; REDDIHOUGH DS
      6 MONTH FOLLOW-UP - THE CRUCIAL TEST OF MULTIDISCIPLINARY DEVELOPMENTAL ASSESSMENT

      Child care health and development
    100. GRINGRAS P
      CHOICE OF MEDICAL INVESTIGATIONS FOR DEVELOPMENTAL DELAY - A QUESTIONNAIRE SURVEY

      Child care health and development


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/10/20 alle ore 01:11:54