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List of works by William H. McAlister

4p- (Wolf-Hirschhorn) syndrome

scientific article published in August 1980

A radiant-heating device for control of body temperature of infants during radiography

scientific article published on 01 July 1973

Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathy

scientific article published on 01 September 2007

Absence of an osteopetrosis phenotype in IKBKG (NEMO) mutation-positive women: A case-control study

scientific article published on 16 January 2019

Aortic aneurysms in children

scientific article published on September 1, 1979

Asfotase alfa for infants and young children with hypophosphatasia: 7 year outcomes of a single-arm, open-label, phase 2 extension trial

scientific article published on 14 December 2018

Asfotase alfa therapy for children with hypophosphatasia

scientific article

Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease

scientific article published on 14 January 2016

Axial Radiography of the Spine: A Projection for Evaluation of the Neural Arches in Children ⬇️

scientific article published on March 1, 1979

Bilateral radial ray hypoplasia with multiple epiphyseal dysplasia

scientific article published on 01 May 1998

Bisphosphonate-induced osteopetrosis

scientific article published in July 2003

Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases

scientific article published in October 2008

Brachytelephalangic chondrodysplasia punctata with marked cervical stenosis and cord compression: report of two cases

scientific article published on 02 February 2002

Branchial fistula: CT manifestations

scientific article published on January 1, 1992

Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation

scientific article published on 28 August 2019

COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.

scientific article

CT manifestations of ileal dysgenesis

scientific article published on 9 November 2006

Calcinosis Universalis Complicating Juvenile Dermatomyositis: Resolution During Probenecid Therapy1 ⬇️

scientific article published on 01 November 1997

Calyceal Diverticula in Children: Unusual Features and Complications ⬇️

scientific article published on April 1, 1979

Cantu syndrome

scientific article published on 27 February 2005

Cartilaginous esophageal ring: a cause of esophageal stenosis in infants and children

scientific article

Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature

scientific article published on December 1989

Chest wall deformity and respiratory distress in a 17-year-old patient with achondroplasia: CT and MRI evaluation

scientific article published on 01 January 1992

Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia

scientific article published on 01 August 2009

Circular esophageal myotomy simulating a pulmonary or mediastinal pseudocyst

scientific article published on 01 August 1980

Classification of spinal curvatures

scientific article published on 01 April 1975

Coalescing Expansile Skeletal Disease: Delineation Of An Extraordinary Osteopathy Involving The IFITM5 Mutation Of Osteogenesis Imperfecta Type V

scientific article published on 24 December 2020

Combined deficiency of beta-galactosidase and neuraminidase: natural history of the disease in the first 18 years of an American patient with late infantile onset form

scientific article (publication date: December 1990)

Complications associated with cystography in children

scientific article published on 01 April 1974

Computed radiography versus screen-film radiography: detection of pulmonary edema in a rabbit model that simulates neonatal pulmonary infiltrates

scientific article published on 01 November 1999

Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.

scientific article published on 30 December 2015

Congenital intraspinal neuroblastoma: a treatable simulant of myelodysplasia

scientific article published on 01 January 1982

Congenital mesoblastic nephroma

scientific article published on 01 August 1979

Congenital occipital dermal sinus

scientific article published in April 1974

Craniosynostosis: diagnostic imaging with three-dimensional CT presentation.

scientific article published in November 1994

Craniosynostosis: diagnostic value of three-dimensional CT reconstruction

scientific article

Cysts of the omentum ⬇️

scientific article published on June 13, 1975

Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis

scientific article

Dedifferentiated chondrosarcoma in childhood: report of a case

scientific article published on 01 November 1995

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification

scientific article published in November 2000

Desmoplastic nested spindle cell tumor of liver: report of four cases of a proposed new entity

scientific article published on January 2005

Differing Lumbar Vertebral Mineralization Rates in Ambulatory Pediatric Patients with Osteogenesis Imperfecta ⬇️

scientific article published on January 1, 1998

Dyskeratosis congenita

scientific article published on 01 March 1997

Dysosteosclerosis presents as an "osteoclast-poor" form of osteopetrosis: comprehensive investigation of a 3-year-old girl and literature review.

scientific article

Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders

scientific article published in November 2010

Enzyme replacement therapy for infantile hypophosphatasia attempted by intravenous infusions of alkaline phosphatase-rich Paget plasma: results in three additional patients

scientific article

Enzyme-replacement therapy in life-threatening hypophosphatasia.

scientific article published in March 2012

Erratum: Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndrome (Pediatr Radiol (1997) 27: 436-441) ⬇️

scientific article published on 01 November 1997

Esophageal diverticula in childhood associated with strictures from unsuspected foreign bodies of the esophagus ⬇️

scientific article published on January 1, 1991

Expansile skeletal hyperphosphatasia: a new familial metabolic bone disease

scientific article published in December 2000

Fibrous bowel adhesion simulating recurrence of Hodgkin's disease ⬇️

scientific article published on February 1, 1976

Focal fibrocartilaginous dysplasia associated with tibia vara

scientific article published on 01 December 1990

Gastrointestinal and renal abnormalities in cardio-facio-cutaneous syndrome

scientific article published on 15 October 2004

Genetic heterogeneity in multiple lysosomal hydrolase deficiency

scientific article published on 01 August 1974

Genetics casebook. X-linked dominant chrondrodyplasia punctata without stippled epiphyses

scientific article published on 01 March 1997

Glomerulocystic kidney ⬇️

scientific article published on September 1, 1979

Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5).

scientific article published on 21 November 2017

Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health

scientific article published on 18 March 2020

Henoch-Schonlein syndrome in children: gastrointestinal manifestations

scientific article published on 01 June 1981

High costs of low-osmolality contrast media ⬇️

scientific article published on 01 September 1995

Hyperalimentation catheter passing into the spinal canal causing temporary paraplegia ⬇️

scientific article published on June 19, 1978

Hypercalciuria in osteogenesis imperfecta: a follow-up study to assess renal effects

scientific article published in March 1995

Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review) ⬇️

scientific article published on October 1, 2011

Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patients

scientific article published on 27 February 2015

Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding osteopontin: The first digenic SIBLING protein osteopathy?

scientific article published on 13 December 2019

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome

scientific article published in July 1990

Infantile hypophosphatasia: enzyme replacement therapy by intravenous infusion of alkaline phosphatase-rich plasma from patients with Paget bone disease

scientific article

Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblasts

scientific article

Inherited diseases of bone density in children

scientific article published on January 1991

Intermittent radiographic changes of rickets without defective trabecular bone mineralization in a case of spondylometaphyseal dysplasia

scientific article published in January 1986

Intestinal perforations by tube feedings in small infants: clinical and experimental studies

scientific article published on 01 October 1985

Intestinal stricture in necrotizing enterocolitis

scientific article published on June 1, 1976

Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor Sp7)

scientific article published on 13 April 2020

Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation ⬇️

scientific article published on June 1, 2013

Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK

scientific article

Juvenile paget disease: Life-long features of a mildly affected young woman

article

Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes

scientific article published on 15 November 2018

Left-sided congenital diaphragmatic hernia: delayed presentation

scientific article published on 01 July 1981

Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1.

scientific article published in April 2015

Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive condition

scientific article published in January 1986

Malignant small cell tumor of the thoracopulmonary region in childhood.A distinctive clinicopathologic entity of uncertain histogenesis ⬇️

scientific article published on June 1, 1979

Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes).

scientific article published in September 2000

Marrow cell transplantation for infantile hypophosphatasia

scientific article (publication date: April 2003)

Measurement of spinal curvatures

scientific article published on 01 April 1975

Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS.

scientific article published on 20 April 2017

Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864

scientific article published on 01 May 1997

Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.

scientific article

Multifocal synchronous osteosarcoma with cutaneous and muscle metastases

scientific article

Neonatal High Bone Mass With First Mutation of the NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65).

scientific article published on 14 July 2015

Neonatal Meconium Blockage in the Ileum and Proximal Colon ⬇️

scientific article published on July 1, 1979

Neonatal mucolipidosis II (I-cell disease) with dysharmonic epiphyseal ossification and butterfly vertebral body

scientific article

Neonatal umbilical artery pseudoaneurysm: sonographic evaluation (case report)

scientific article published on 01 August 1986

New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6

scientific article published on 11 May 2019

No vascular calcification on cardiac computed tomography spanning asfotase alfa treatment for an elderly woman with hypophosphatasia

scientific article published on 28 February 2019

Non-Endemic Skeletal Fluorosis: Causes And Associated Secondary Hyperparathyroidism (Case Report and Literature Review)

scientific article published on 05 January 2021

Occipital horn syndrome. Additional radiographic findings in two new cases

scientific article published on January 1, 1992

Osteopetrosis, renal tubular acidosis and basal ganglia calcification in three sisters

scientific article published on July 1980

Osteoprotegerin deficiency and juvenile Paget's disease

scientific article

PAGOD syndrome: a new abdominal finding and risk of sudden death

scientific article published in May 2005

PHEX 3'-UTR c.*231A>G near the polyadenylation signal is a relatively common, mild, American mutation that masquerades as sporadic or X-linked recessive hypophosphatemic rickets

scientific article published in January 2015

Panostotic expansile bone disease with massive jaw tumor formation and a novel mutation in the signal peptide of RANK.

scientific article published on April 2014

Paranasal sinus mucoceles in children

scientific article published on 01 December 1979

Pediatric radiology case of the day. Congenital hepatic fibrosis with saccular dilatation of the intrahepatic bile ducts and infantile polycystic kidneys

scientific article published on 01 June 1989

Pediatric radiology case of the day. Diffuse infiltrating lipomatosis

scientific article published on 01 June 1989

Pediatric radiology case of the day. Duodenal duplication

scientific article published on 01 June 1989

Pediatric radiology case of the day. Oncogenic rickets (Feuerstein and Mims syndrome with resistant rickets)

scientific article published on 01 June 1989

Peripheral primitive neuroectodermal tumor: report of a case arising in the kidney ⬇️

scientific article published on 01 July 1997

Perlman syndrome: report of a case with additional radiographic findings

scientific article published on 01 November 1995

Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy

scientific article published on 28 May 2020

Pleural thickening. An unusual feature of childhood leukemia

scientific article published on 01 February 1981

Pneumoperitoneography in the Evaluation of Congenital Anomalies in the Umbilical Region ⬇️

scientific article published on 01 August 1972

Polycystic bone disease

scientific article published on 01 February 2000

Polycystic bone disease: A new, autosomal dominant disorder

scientific article published on 01 August 1999

Posterior mediastinal capillary hemangioma with extradural extension resembling neuroblastoma

scientific article published on 01 July 1999

Preonset Studies of Spondyloepiphyseal Dysplasia Tarda Caused by a Novel 2-Base Pair Deletion in SEDL Encoding Sedlin ⬇️

scientific article published on 01 December 2001

Pseudo-(tumor-induced) rickets

scientific article

Pseudotumoral sarcoid granulomatous nephritis in a child: case presentation with sonographic and CT findings ⬇️

scientific article published on 01 September 1997

Pulmonary oedema following intravenous urography in a neonate ⬇️

scientific article published on May 1, 1979

Pulmonary venoocclusive disease: case report and review of the literature

scientific article published on April 1, 1977

Radiographic findings in ovarian teratomas in children ⬇️

scientific article published on October 1, 1978

Radiographic manifestations of congenital anomalies of the lower urinary tract

scientific article published on March 1991

Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660).

scientific article

Rapid skeletal turnover in a radiographic mimic of osteopetrosis.

scientific article

Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic Mastocytosis

scientific article published on 10 June 2015

Response to: A Rapid Skeletal Turnover in Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic Mastocytosis

article

SAT-LB085 First Report of Burosumab (Anti-FGF23 Monoclonal Antibody) for Rickets Complicating HRAS-Associated Cutaneous Skeletal Hypophosphatemia Syndrome

scientific article published on 30 April 2019

Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review

scientific article published on 02 August 2018

Serum concentrations of 25-hydroxyvitamin D in rickets of extremely premature infants

scientific article published on March 1, 1979

Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy ⬇️

scientific article published on February 1, 2013

Sinus histiocytosis: some radiologic observations ⬇️

scientific article published on May 1, 1979

Skeletal Fluorosis Due To Inhalation Abuse of a Difluoroethane-Containing Computer Cleaner.

scientific article

Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?

scientific article published in December 2005

Skeletal surveys for child abuse: comparison of interpretation using digitized images and screen-film radiographs ⬇️

scientific article published on November 1, 1998

Soft-copy versus hard-copy cranial sonography: intraobserver agreement and workstation efficiency ⬇️

scientific article published on August 1, 1997

Special imaging casebook. Hereditary tyrosinemia, acute type I

scientific article published on 01 January 1997

Spondyloepimetaphyseal dysplasia: clinical and radiologic investigation of a large kindred manifesting autosomal dominant inheritance, and a review of the literature.

scientific article published on September 1993

Subglottic edema in acute epiglottitis in children

scientific article published on October 1978

The "pop-top" tab. A cause of esophageal stenosis

scientific article published on 01 January 1975

The Use of a Foley Catheter for Removal of Blunt Esophageal Foreign Bodies from Children ⬇️

scientific article published on 01 November 1972

The position and mobility of the duodenum in children

scientific article published on 01 May 1987

The rectosigmoid index

scientific article published on 01 May 1981

The small liver: A radiographic feature of fatal neonatal cirrhosis ⬇️

scientific article published on November 15, 1979

Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic rickets

scientific article published in February 1987

Tracheal bronchus

scientific article published on 01 February 1979

Tubular communicating duplications of esophagus and stomach ⬇️

scientific article published on 01 January 1991

Ulcerative and granulomatous colitis in children. Comparison of double- and single-contrast studies

scientific article published on 01 March 1985

Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis

scientific article published on 30 July 2018

Unusual intrathoracic complications in Wilms tumor

scientific article published on 01 June 1980

Upper airway and external genital involvement in epidermolysis bullosa dystrophica

scientific article published on 01 May 1982

Validation of a Novel Scoring System for Changes in Skeletal Manifestations of Hypophosphatasia in Newborns, Infants, and Children: The Radiographic Global Impression of Change Scale

scientific article published on 3 January 2018

X-linked hypophosphatemia: Normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-induced renal azotemia ⬇️

scientific article published on December 1, 1997

X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature

scientific article published in January 1999

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