V. Ionasescu

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Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

K. Fischbeck, E. Green, J. Vance, 2003, American journal of human genetics.

Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNAPro gene

S. Dimauro, M. Hart, C. Moraes, 1994, Neurology.

Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy.

Nancy F. Hansen, J. Lupski, J. Mullikin, 2010, American journal of human genetics.

Teratogenic effect of anticonvulsant drugs.

V. Ionasescu, H. Zellweger, M. Waziri, 1976, American journal of diseases of children.

Magnetic resonance imaging of children with Duchenne muscular dystrophy

Wilbur L. Smith, J. Ehrhardt, E. Franken, 2006, Pediatric Radiology.

The human connexin32 gene is transcribed from two tissue-specific promoters

R. Werner, V. Ionasescu, L. Bone, 1996, Bioscience reports.

Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy.

V. Ionasescu, C. Searby, R. Ionasescu, 1994, Human molecular genetics.

Screening of dominantly inherited Charcot–Marie–Tooth neuropathies

V. Ionasescu, C. Searby, R. Ionasescu, 1993, Muscle & nerve.

Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplication.

D. Barker, V. Ionasescu, C. Searby, 1993, Human molecular genetics.

DETECTION of CARRIERS and GENETIC COUNSELING IN DUCHENNE MUSCULAR DYSTROPHY BY RIBOSOMAL PROTEIN SYNTHESIS

V. Ionasescu, H. Zellweger, L. Burmeister, 1976, Acta neurologica Scandinavica.

Twenty years-iowa muscle clinic: Reminiscences and prospects

V. Ionasescu, H. Zellweger, J. Simpson, 1982, European Journal of Pediatrics.

Becker muscular dystrophy recombinant DNA studies in identical twins

V. Ionasescu, C. Searby, R. Ionasescu, 1988, Muscle and Nerve.

Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2).

R. Ferrell, V. Ionasescu, C. Searby, 1988, American journal of human genetics.

Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1.

A. Whitehead, V. Ionasescu, C. Searby, 1988, Cytogenetics and cell genetics.

Localization of the gene for X‐linked spinal muscular atrophy

K. Fischbeck, K. Davies, I. Hausmanowa-Petrusewicz, 1986, Neurology.

SERIAL POSITION MEMORY OF BOYS WITH DUCHENNE MUSCULAR DYSTROPHY

S. Anderson, D. Routh, V. Ionasescu, 1988, Developmental medicine and child neurology.

Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation.

R. Folberg, V. Ionasescu, H. Yi, 1993, Ophthalmology.

Letters to te editor

C. Gravel, C. Pozzilli, G. Gronseth, 1995 .

Charcot–marie–tooth neuropathies: From clinical description to molecular genetics

V. Ionasescu, V V Ionasescu, 1995, Muscle & nerve.

A Dejerine‐Sottas neuropathy family with a gene mapped on chromosome 8

V. Ionasescu, M. Ross, C. Searby, 1996, Muscle & nerve.

Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B.

K. Hayasaka, V. Ionasescu, G. Takada, 1993, Human molecular genetics.

STUDIES ON CARBOHYDRATE METABOLISM IN AMYOTROPHIC LATERAL SCLEROSIS AND HEREDITARY PROXIMAL SPINAL MUSCULAR ATROPHY

V. Ionasescu, N. Luca, 1964, Acta neurologica Scandinavica.

Human smooth muscle cell cultures of the stomach morphologic and biochemical studies

V. Ionasescu, R. Ionasescu, 1985, In Vitro Cellular & Developmental Biology.

Dejerine‐Sottas neuropathy in mother and son with same point mutation of PMP22 gene

V. Ionasescu, S. Chatkupt, C. Searby, 1997, Muscle & nerve.

Inherited ophthalmoplegia with intestinal pseudo-obstruction

V. Ionasescu, F. Mitros, C. Searby, 1983, Journal of the Neurological Sciences.

DUCHENNE MUSCULAR DYSTROPHY IN YOUNG GIRLS?

V. Ionasescu, H. Zellweger, 1974, Acta neurologica Scandinavica.

Frequency of new mutants among boys with Duchenne muscular dystrophy.

V. Ionasescu, K. Bucher, J. Hanson, 1980, American journal of medical genetics.

Late-onset oculogastrointestinal muscular dystrophy.

H. S. Thompson, V. Ionasescu, C. Aschenbrener, 1984, American journal of medical genetics.

Oculogastrointestinal muscular dystrophy.

V. Ionasescu, V. Ionasescu, J. M. Opitz, 1983, American journal of medical genetics.

X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene

R. Stevenson, A. Rosenthal, S. Kenwrick, 1994, Nature Genetics.

Myotonic Dystrophy and its Differential Diagnosis

V. Ionasescu, H. Zellweger, 1973, Acta neurologica Scandinavica. Supplementum.

The role of collagen in the pathogenesis of idiopathic clubfoot. Biochemical and electron microscopic correlations.

V. Ionasescu, I. Ponseti, H. Zellweger, 1974, Helvetica paediatrica acta.

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

K. Buetow, K. Mathews, J. Murray, 1992, American journal of human genetics.

Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy

R. Werner, V. Ionasescu, C. Searby, 1996, Neurology.

High resolution gene mapping of the human alpha globin locus.

D. Weatherall, D. Higgs, R. Nicholls, 1987, Journal of medical genetics.

locus . of the human alpha globin High resolution gene mapping

D. Weatherall, D. Higgs, R. Nicholls, 2022 .

High resolution gene mapping of the human oa globin locus

D. Weatherall, R. Nicholls, V. Ionasescu, 2004 .

[Genetic neurological diseases].

V. Ionasescu, C. Rosianu, M. Drincă-Ionescu, 1967, Studii si cercetari de neurologie.

The Problem of Trisomy 22

V. Ionasescu, H. Zellweger, L. Burmeister, 1976, Clinical pediatrics.

Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy

K. E. Davies, Pascale Briand, V. Ionasescu, 1985, Nucleic Acids Res..

RECOMBINATION WITH PERT87 (DXS164) IN FAMILIES WITH X-LINKED MUSCULAR DYSTROPHY

M. Pericak-Vance, C. Bertelson, K. Fischbeck, 1986, The Lancet.

Trisomy 22.

V. Ionasescu, H. Zellweger, J. Simpson, 1975, Journal de genetique humaine.

Ribosomal protein synthesis in Duchenne muscular dystrophy.

V. Ionasescu, H. Zellweger, T. Conway, 1971, Archives of biochemistry and biophysics.

Gastrointestinal manifestations of the muscular dystrophies

V. Ionasescu, T. Nowak, S. Anuras, 1982 .

Carrier detection in Duchenne muscular dystrophy

V. Ionasescu, K. Bucher, 1980 .

A new approach for carrier detection in Duchenne muscular dystrophy

V. Ionasescu, H. Zellweger, T. Conway, 1971, Neurology.

Fibroblast clones for detection of Duchenne carriers.

V. Ionasescu, C. Searby, R. Ionasescu, 1983, The New England journal of medicine.

Increased collagen synthesis by Duchenne myogenic clones

V. Ionasescu, R. Ionasescu, 1982, Journal of the Neurological Sciences.

Collagen synthesis by Duchenne myogenic clones: pathogenic implications for the disease.

V. Ionasescu, A. Sandra, G. Massimini, 1982, American journal of medical genetics.

Alterations in lipid incorporation in Duchenne muscular dystrophy Studies of fresh and cultured muscle

L. Stern, V. Ionasescu, A. Sandra, 1981, Journal of the Neurological Sciences.

Discriminant analysis of ribosomal protein synthesis findings in carrier detection of Duchenne muscular dystrophy.

V. Ionasescu, L. Burmeister, J. Hanson, 1980, American journal of medical genetics.

Stimulatory effects of drugs for protein synthesis on muscle cell cultures in duchenne dystrophy

L. Stern, V. Ionasescu, P. Rubenstein, 1979, Annals of neurology.

FIBROBLAST CULTURES IN DUCHENNE MUSCULAR DYSTROPHY

V. Ionasescu, H. Zellweger, L. Burmeister, 1977 .

PROTEIN SYNTHESIS IN MUSCLE CULTURES FROM PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY

V. Ionasescu, P. Cancilla, H. Zellweger, 1976, Acta neurologica Scandinavica.

Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis.

V. Ionasescu, 1975, Journal of medical genetics.

Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy

V. Ionasescu, H. Zellweger, T. Conway, 1974, Journal of medical genetics.

Hypokalemic periodic paralysis: Low activity of sarcoplasmic reticulum and muscle ribosomes during an induced attack

V. Ionasescu, S. Schochet, T. Conway, 1974 .

Biochemical abnormalities of muscle ribosomes during attacks of hyperkalemic periodic paralysis.

V. Ionasescu, S. Schochet, H. Zellweger, 1973, Journal of the neurological sciences.

Increased collagen synthesis in arthrogryposis multiplex congenita.

L. Filer, V. Ionasescu, H. Zellweger, 1970, Archives of neurology.

Glycogenosis. IV. A new cause of infantile hypotonia.

V. Ionasescu, W. Mccormick, S. Schochet, 1972, The Journal of pediatrics.

Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature.

V. Ionasescu, W. Mccormick, S. Schochet, 1972, Journal of the neurological sciences.

Early onset of myotonic dystrophy in infants.

V. Ionasescu, H. Zellweger, 1973, American journal of diseases of children.

Small intestinal motility in myotonic dystrophy patients.

V. Ionasescu, T. Nowak, B. Brown, 1984, Gastroenterology.

Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination.

M. Ruberg, A. Brice, N. Lévy, 1998, Human molecular genetics.

Report of a new kindred

V. Ionasescu, W. Mccormick, H. Zellweger, 2006 .

Gastrointestinal manifestations of the muscular dystrophies.

V. Ionasescu, T. Nowak, S. Anuras, 1982, Gastroenterology.

X‐linked dominant charcot–marie–tooth neuropathy with 15 cases in a family genetic linkage study

V. Ionasescu, C. Searby, R. Ionasescu, 1988, Muscle & nerve.

Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality.

V. Ionasescu, W. Rhead, W. Smith, 1987, American journal of medical genetics.

Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

V. Sheffield, V. Ionasescu, C. Searby, 1996, Human molecular genetics.

Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 gene.

S. Greenberg, V. Ionasescu, C. Searby, 1996, Journal of medical genetics.

A mitochondrial tRNA anticodon swap associated with a muscle disease

S. Dimauro, E. Schon, C. Moraes, 1993, Nature Genetics.

The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical map.

V. Sheffield, J. McPherson, E. Green, 1999, Genome research.

Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.

J. Haines, A. Summers, J. Trofatter, 1991, American journal of human genetics.

Linkage studies of X-linked recessive spastic paraplegia using DNA probes

K. Davies, S. Kenwrick, V. Ionasescu, 1986, Human Genetics.

A familial visceral myopathy with external ophthalmoplegia and autosomal recessive transmission.

V. Ionasescu, F. Mitros, T. Nowak, 1983, Gastroenterology.

Drug trial of superoxide dismutase in Duchenne's muscular dystrophy.

R. J. Pellegrino, L. Stern, V. Ionasescu, 1982, Archives of neurology.

Genetics in Neurology

V. Ionasescu, H. Zellweger, 1983 .

Giant axonal neuropathy: normal protein composition of neurofilaments.

V. Ionasescu, P. Cancilla, P. Rubenstein, 1983, Journal of neurology, neurosurgery, and psychiatry.

Duchenne muscular dystrophy

J. Towbin, S. W. Sernett, K. Campbell, 1993, Neurology.

Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.

J. Ervasti, K. Campbell, N. Romero, 1993, The Journal of clinical investigation.

The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies

K. Campbell, I. Nonaka, J. Kaplan, 1993, Neuromuscular Disorders.

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.

K. Fischbeck, E. Green, M. Dalakas, 2005, Brain : a journal of neurology.

Severe Charcot‐Marie‐Tooth neuropathy type 1A with 1‐base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene

V. Ruggieri, V. Ionasescu, R. Reisin, 1997, Muscle & nerve.

Autosomal recessive generalized myotonia

R. Schieken, L. Pavone, V. Ionasescu, 1980, Muscle & nerve.

Alterations in lipid turnover in developing muscle.

V. Ionasescu, A. Sandra, 1980, Biochemical and Biophysical Research Communications - BBRC.

Schwartz-Jampel Syndrome: a Case Report

V. Ionasescu, N. Scribanu, 1981 .

RESPIRATORY CONTROL AND OXIDATIVE PHOSPHORYLATION IN THE DYSTROPHIC MUSCLE

V. Ionasescu, O. Vuia, N. Luca, 1967, Acta neurologica Scandinavica.

Frequency of cerebral infarction in patients with inherited neuromuscular diseases.

H. Adams, J. Biller, V. Ionasescu, 1987, Stroke.

RESPIRATORY CONTROL AND OXIDATIVE PHOSPHORYLATION IN THE DENERVATED MUSCLE OF PATIENTS WITH AMYOTROPHIC LATERAL SCLEROSIS

V. Ionasescu, V. Popa, O. Vuia, 1968, Acta neurologica Scandinavica.

STUDIES ON CARBOHYDRATE METABOLISM IN MUSCULAR DISEASES IN CONDITIONS OF ISCHAEMIC WORK.

V. Ionasescu, N. Luca, 1965, Psychiatria et neurologia.

Intestinal pseudo‐obstruction in adult spinal muscular atrophy

V. Ionasescu, J. Christensen, M. Hart, 1994, Muscle & nerve.

Spinal muscular atrophy with autosomal dominant inheritance

V. Ionasescu, W. Mccormick, H. Zellweger, 1972, Neurology.

Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene

V. Ionasescu, C. Searby, R. Ionasescu, 1995, Neurology.

Prenatal diagnosis of Duchenne muscular dystrophy based on Xp21.2 deletion

V. Ionasescu, C. Searby, R. Ionasescu, 1986, Neurology.

Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.

C. Hoppel, V. Ionasescu, G. Hug, 1980, Journal of neurology, neurosurgery, and psychiatry.

Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy.

V. Ionasescu, C. Searby, R. Ionasescu, 1996, American journal of medical genetics.

Amino acid abnormality in Sjögren-Larsson syndrome.

V. Ionasescu, L. Stegink, M. Weinstein, 1973, Archives of neurology.

X‐LINKED CHARCOT‐MARIE‐TOOTH DISEASE AND CONNEXIN32

V. Ionasescu, 1998, Cell biology international.

Mapping of the gene for X‐linked dominant Charcot‐Marie‐Tooth neuropathy

J. Haines, J. Trofatter, V. Ionasescu, 1992, Neurology.

Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies

V. Ionasescu, C. Searby, R. Ionasescu, 1989, Acta neurologica Scandinavica.

FETAL SERUM-CREATINE-PHOSPHOKINASE NOT A VALID PREDICTOR OF DUCHENNE MUSCULAR DYSTROPHY

V. Ionasescu, P. Cancilla, Hans Zelleger, 1978, The Lancet.

PAROXYSMAL DISORDERS OF THE BODY IMAGE IN TEMPORAL LOBE EPILEPSY

V. Ionasescu, 1960, Acta psychiatrica Scandinavica.

Identification of carriers of Duchenne muscular dystrophy by muscle protein synthesis

V. Ionasescu, P. Shirk, T. Conway, 1973, Neurology.

New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy

W. Meschino, V. Ionasescu, C. Searby, 1995, Neuromuscular Disorders.

Dominantly inherited dilated cardiomyopathy.

D. Skorton, L. Mahoney, V. Ionasescu, 1987, American journal of medical genetics.

A CASE OF `PURE' WORD BLINDNESS

A. Kreindler, V. Ionasescu, 1961, Journal of neurology, neurosurgery, and psychiatry.

Letters to te editor

C. Pozzilli, G. Gronseth, Y. Péréon, 1995 .

Muscular dystrophy research: From molecular diagnosis toward therapy. Editors: C. Angelini, GA Danieli, and D. Fontanari, Elsevier Science Publishers, Amsterdam, 1991 273 pp

V. Ionasescu, 1992 .

Charcot-Marie-Tooth neuropathy related to chromosome 1.

J. Haines, J. Trofatter, V. Ionasescu, 1992, American journal of medical genetics.

X‐linked recessive Charcot–Marie‐Tooth neuropathy: Clinical and genetic study

J. Haines, A. Summers, J. Trofatter, 1992, Muscle & nerve.

HEREDITARY PROXIMAL SPINAL MUSCULAR ATROPHY. BIOCHEMICAL INVESTIGATIONS.

V. Ionasescu, G. Calcaianu, N. Luca, 1965, Confinia neurologica.

NEUROGENIC CONTROL OF MUSCLE RIBOSOMAL PROTEIN SYNTHESIS

V. Ionasescu, Ruth E. Lewis, Victor Ionasescu, 1975, Acta neurologica Scandinavica.

INVESTIGATIONS ON CARBOHYDRATE METABOLISM IN PROGRESSIVE MUSCULAR DYSTROPHIES.

V. Ionasescu, N. Luca, 1963, Psychiatria et neurologia.

Teratogenic effect of anticonvulsant drugs.

V. Ionasescu, H. Zellweger, M. Waziri, 1976, American journal of diseases of children.

Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I)

J. Chirgwin, J. Murray, V. Ionasescu, 1987, Journal of the Neurological Sciences.